Enhancers that have rs186392867[chr14:61573744]
Back to top

Transcript factors that have rs186392867[chr14:61573744]
Back to top
Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 61573119 61574722 ZNF274 GTRD no Cervix (HeLa-S3) 21621902
chr14 61573166 61574904 ZNF274 GTRD no Cervix (HeLa-S3) 21621903
chr14 61573438 61574693 ZNF274 GTRD no Cervix (HeLa-S3) 21621904
chr14 61573542 61573832 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21621905
chr14 61573548 61573818 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21621906
chr14 61573562 61573822 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21621907
chr14 61573573 61573803 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21621908
chr14 61573593 61573817 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21621909
chr14 61573600 61573850 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21621910
chr14 61573663 61574654 ZNF274 GTRD no Cervix (HeLa-S3) 21621911
chr14 61573686 61575081 P63 GTRD no Skin (Keratinocyte) 21621912
chr14 61573701 61574636 ZNF274 GTRD no Cervix (HeLa-S3) 21621913
chr14 61573729 61573744 HNF4A JASPAR yes 115816586
chr14 61573740 61573754 RXRB JASPAR yes 115816587
chr14 61573740 61573754 RXRG JASPAR yes 115816588
chr14 61573740 61573755 NR2C2 JASPAR yes 115816589

Genes associated with rs186392867[chr14:61573744], comfirmed by eQTL
Back to top
Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More