Enhancers that have rs142890653[chr19:770226]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 766416 774574 enh32870

Transcript factors that have rs142890653[chr19:770226]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 769496 771860 TCF7L2 GTRD no Colon (HCT116) 21829728
chr19 769657 772471 TCF7L2 GTRD no Colon (HCT116) 21829729
chr19 769715 770874 TCF7L2 GTRD no Colon (HCT116) 21829730
chr19 769728 770761 TCF7L2 GTRD no Colon (HCT116) 21829731
chr19 769933 770872 ZNF274 GTRD no Cervix (HeLa-S3) 21829732
chr19 770142 771764 ZNF274 GTRD no Cervix (HeLa-S3) 21829733
chr19 770179 770621 ZNF274 GTRD no Cervix (HeLa-S3) 21829734
chr19 770191 770601 ZNF274 GTRD no Cervix (HeLa-S3) 21829735
chr19 770206 770626 ZNF274 GTRD no Cervix (HeLa-S3) 21829736
chr19 770210 770708 TCF7L2 GTRD no Colon (HCT116) 21829737
chr19 770214 770233 CTCF JASPAR yes 111974528
chr19 770214 770678 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21829738
chr19 770217 770793 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21829739

Genes associated with rs142890653[chr19:770226], 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