# CACHE UPDATED 2016-04-14 16:23:27
sift	b
cell_types	A549,CD14+CD16-Monocyte:CordBlood:hist,CD14+CD16-Monocyte:VenousBlood:hist,CD4+abTcell:VenousBlood:hist,CD8+abTcell:CordBlood:hist,CMCD4+abTcell:VenousBlood:hist,DND-41,eosinophil:VenousBlood:hist,EPC:VenousBlood:hist,erythroblast:CordBlood:hist,GM12878,H1ESC,HeLa-S3,HepG2,HMEC,HSMM,HSMMtube,HUVEC,HUVECprol:CordBlood:hist,IMR90,K562,M0Macrophage:CordBlood:hist,M0Macrophage:VenousBlood:hist,M1Macrophage:CordBlood:hist,M1Macrophage:VenousBlood:hist,M2Macrophage:CordBlood:hist,M2Macrophage:VenousBlood:hist,Monocytes-CD14+,MSC:VenousBlood:hist,naiveBcell:VenousBlood:hist,neutroMyelocyte:BoneMarrow:hist,neutrophil:CordBlood:hist,neutrophil:VenousBlood:hist,NH-A,NHDF-AD,NHEK,NHLF,Osteobl,MultiCell
serialiser_type	sereal
build	all
polyphen	b
regulatory	1
assembly	GRCh38
species	homo_sapiens
source_sift	sift5.2.2
source_polyphen	2.2.2
source_gencode	GENCODE 24
source_genebuild	2014-07
source_regbuild	13.0
source_assembly	GRCh38.p5
variation_cols	chr,variation_name,failed,somatic,start,end,allele_string,strand,minor_allele,minor_allele_freq,clin_sig,phenotype_or_disease,pubmed,AFR,AMR,EAS,EUR,SAS,AA,EA,gnomAD,gnomAD_AFR,gnomAD_AMR,gnomAD_ASJ,gnomAD_EAS,gnomAD_FIN,gnomAD_NFE,gnomAD_OTH,gnomAD_SAS
var_type	tabix
source_COSMIC	80
source_HGMD-PUBLIC	20164
source_ESP	20141103
source_ClinVar	201704
source_dbSNP	149