Enhancers that have rs76710467[chr14:69998800]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 69997445 70012619 enh15729

Transcript factors that have rs76710467[chr14:69998800]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 69997098 70000341 ZNF274 GTRD no Cervix (HeLa-S3) 21626627
chr14 69997444 70000193 ZNF274 GTRD no Cervix (HeLa-S3) 21626634
chr14 69997504 70001488 ZNF274 GTRD no Cervix (HeLa-S3) 21626635
chr14 69998518 69998811 ZNF274 GTRD no Blood (GM12878) 21626646
chr14 69998551 70000257 ZNF274 GTRD no Cervix (HeLa-S3) 21626647
chr14 69998586 70000341 ZNF274 GTRD no Cervix (HeLa-S3) 21626648
chr14 69998617 70000283 ZNF274 GTRD no Cervix (HeLa-S3) 21626649
chr14 69998623 70000825 ZNF274 GTRD no Cervix (HeLa-S3) 21626650
chr14 69998633 70000924 ZNF274 GTRD no Cervix (HeLa-S3) 21626651
chr14 69998689 69999996 ZNF274 GTRD no Cervix (HeLa-S3) 21626652
chr14 69998725 70000340 ZNF274 GTRD no Cervix (HeLa-S3) 21626653
chr14 69998773 70000290 ZNF274 GTRD no Cervix (HeLa-S3) 21626654
chr14 69998794 69998805 HOXA10 JASPAR yes 116305965
chr14 69998795 69998804 CDX1 JASPAR yes 116305966
chr14 69998795 69998806 CDX2 JASPAR yes 116305967

Genes associated with rs76710467[chr14:69998800], comfirmed by eQTL
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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