<opt>
  <data name="EBI - Ensembl GRCh38" alternativeUrl="https://www.ensembl.org" apiVersion="v1.0.1" createDateTime="" description="Human variant data from the Ensembl database" id="org.ensembl.rest" info="" sampleAlleleRequests="" updateDateTime="" version="102" welcomeUrl="https://rest.ensembl.org">
    <datasets name="All failed variations" assemblyId="GRCh38" callCount="" createDateTime="" description="Variations that have failed the Ensembl QC checks" externalUrl="https://www.ensembl.org" id="fail_all" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Genotyping chip variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants which have assays on commercial chips held in ensembl" externalUrl="https://www.ensembl.org" id="all_chips" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_CytoSNP12v1" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Cyto SNP-12 v1 whole genome SNP genotyping chip designed for cytogenetic analysis" externalUrl="https://www.ensembl.org" id="Illumina_CytoSNP12v1" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Affy GenomeWideSNP_6.0" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Affymetrix Genome-Wide Human SNP Array 6.0" externalUrl="https://www.ensembl.org" id="Affy_SNP6" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_Human660W-quad" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Human660W-quad whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="Illumina_660Q" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_1M-duo" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Human1M-duo v3 whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="Illumina_1M-duo" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Affy GeneChip 500K" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Affymetrix GeneChip Human Mapping 500K Array Set" externalUrl="https://www.ensembl.org" id="Affy_500K" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_Cardio-Metabo_Chip" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Cardio-Metabo_Chip genotyping array designed to target variants of interest for metabolic and cardiovascular disease traits" externalUrl="https://www.ensembl.org" id="Cardio-Metabo_Chip" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_HumanOmni1-Quad" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanOmni1-Quad whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="HumanOmni1-Quad" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_HumanHap650Y" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanHap650Y v3.0 whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="HumanHap650Y" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_HumanOmni2.5" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanOmni2.5 4v1 whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="HumanOmni2.5" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_Human610_Quad" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Human610_Quad v1_B whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="Human610_Quad" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_HumanHap550" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina Human550 v3.0 whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="HumanHap550" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_HumanOmni5" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanOmni5v1 whole genome genotyping array designed for association studies" externalUrl="https://www.ensembl.org" id="HumanOmni5" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_ExomeChip" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina ExomeChip genotyping array designed to target variants within exons" externalUrl="https://www.ensembl.org" id="ExomeChip" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Illumina_ImmunoChip" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina ImmunoChip genotyping array designed to target variants of interest for autoimmune and inflammatory diseases" externalUrl="https://www.ensembl.org" id="ImmunoChip" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="HumanOmniExpress" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanOmniExpress 12v1-1_a whole genome genotyping array" externalUrl="https://www.ensembl.org" id="HumanOmniExpress" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="All phenotype/disease-associated variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants that have been associated with a phenotype or a disease" externalUrl="https://www.ensembl.org" id="ph_variants" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="OMIM phenotype variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants linked to entries in the Online Mendelian Inheritance in Man (OMIM) database" externalUrl="https://www.ensembl.org" id="ph_omim" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Uniprot variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants with annotations provided by UniProt" externalUrl="https://www.ensembl.org" id="ph_uniprot" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="NHGRI-EBI catalog phenotype variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants associated with phenotype data from the NHGRI-EBI GWAS catalog [http://www.ebi.ac.uk/gwas/]" externalUrl="https://www.ensembl.org" id="ph_nhgri" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="PhenCode" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the PhenCode Project" externalUrl="https://www.ensembl.org" id="phencode" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="COSMIC phenotype variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Phenotype annotations of somatic mutations found in human cancers from the COSMIC project" externalUrl="https://www.ensembl.org" id="ph_cosmic" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="HGMD-PUBLIC variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants annotated by HGMD" externalUrl="https://www.ensembl.org" id="ph_hgmd_pub" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="All ClinVar" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants with ClinVar annotation" externalUrl="https://www.ensembl.org" id="ClinVar" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Clinically associated variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants described by ClinVar as being probable-pathogenic, pathogenic, drug-response or histocompatibility" externalUrl="https://www.ensembl.org" id="clin_assoc" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="dbPEX" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the PEX Gene Database" externalUrl="https://www.ensembl.org" id="dbPEX" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="KAT6BDB" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the K(lysine) acetyltransferase 6B database, BCM" externalUrl="https://www.ensembl.org" id="KAT6BDB" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="HbVar" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants for the Human Hemoglobin Variants and Thalassemias database" externalUrl="https://www.ensembl.org" id="HbVar" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="LMDD" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Leiden Muscular Dystrophy Database" externalUrl="https://www.ensembl.org" id="LMDD" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="OIVD" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Osteogenesis Imperfecta Variant Database" externalUrl="https://www.ensembl.org" id="OIVD" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="PAHdb" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Phenylalanine hydroxylase database" externalUrl="https://www.ensembl.org" id="PAHdb" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="Infevers" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the registry of Hereditary Auto-inflammatory Disorders Mutations" externalUrl="https://www.ensembl.org" id="Infevers" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="HumanCoreExome-12" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the Illumina HumanCoreExome-12 v1 genotyping chip." externalUrl="https://www.ensembl.org" id="HumanCoreExome" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="All LSDB-associated variants" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants association from one or several Locus Specific DataBase (LSDB)" externalUrl="https://www.ensembl.org" id="lsdb_variants" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - All" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - EUR - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in European individuals by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_eur_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - SAS - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in East Asian individuals by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_sas_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - EAS - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in East Asian individuals by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_eas_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - AMR - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in admixed American individuals by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_amr_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - AFR - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in African individuals by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_afr_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - All - common" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped by the 1000 Genomes project (phase 3) with frequency of at least 1%" externalUrl="https://www.ensembl.org" id="1kg_3_com" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - EUR" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in European individuals by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3_eur" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - SAS" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in South Asian individuals by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3_sas" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - EAS" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in East Asian individuals by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3_eas" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - AFR" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in African individuals by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3_afr" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="1000 Genomes 3 - AMR" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants genotyped in admixed American individuals by the 1000 Genomes project (phase 3)" externalUrl="https://www.ensembl.org" id="1kg_3_amr" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="ESP_6500" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants from the NHLBI Exome Sequencing Project (investigating heart, lung and blood disorders)" externalUrl="https://www.ensembl.org" id="esp_6500" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="ExAC" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants identified by the Exome Aggregation Consortium (ExAC) - release 0.3" externalUrl="https://www.ensembl.org" id="exac" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <datasets name="gnomAD" assemblyId="GRCh38" callCount="" createDateTime="" description="Variants reported by the Genome Aggregation Database" externalUrl="https://www.ensembl.org" id="gnomAD" info="" sampleCount="" updateDateTime="" variantCount="" version="102" />
    <organization name="EMBL European Bioinformatics Institute" address="EMBL-EBI, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SD, UK" contactUrl="https://www.ebi.ac.uk/support/" description="The European Bioinformatics Institute (EMBL-EBI) is part of EMBL, an international, innovative and interdisciplinary research organisation funded by 26 member states and two associate member states to provide the infrastructure needed to share data openly in the life sciences." id="ebi" info="" logoUrl="" welcomeUrl="https://www.ebi.ac.uk/" />
  </data>
</opt>
