Enhancers that have rs35382723[chr14:103528244]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs35382723[chr14:103528244]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 103526361 103531110 ZNF143 GTRD no Epithelial (MCF-7) 21642725
chr14 103527221 103533644 ZNF143 GTRD no Epithelial (MCF-7) 21642726
chr14 103527278 103533285 ZNF143 GTRD no Epithelial (MCF-7) 21642727
chr14 103527409 103530313 TCF7L2 GTRD no Colon (HCT116) 21642728
chr14 103527490 103532178 TCF7L2 GTRD no Colon (HCT116) 21642729
chr14 103527561 103531299 ZNF143 GTRD no Epithelial (MCF-7) 21642730
chr14 103527649 103531417 ZNF143 GTRD no Epithelial (MCF-7) 21642731
chr14 103527657 103530935 ZNF143 GTRD no Epithelial (MCF-7) 21642732
chr14 103527772 103530983 ZNF143 GTRD no Epithelial (MCF-7) 21642733
chr14 103527781 103530323 ZNF143 GTRD no Epithelial (MCF-7) 21642734
chr14 103527797 103531049 ZNF143 GTRD no Epithelial (MCF-7) 21642735
chr14 103527829 103529762 ZNF143 GTRD no Epithelial (MCF-7) 21642736
chr14 103527864 103529034 ZNF274 GTRD no Cervix (HeLa-S3) 21642737
chr14 103527882 103530114 ZNF143 GTRD no Epithelial (MCF-7) 21642738
chr14 103527940 103529916 ZNF274 GTRD no Cervix (HeLa-S3) 21642739
chr14 103528071 103529616 TCF7L2 GTRD no Colon (HCT116) 21642740
chr14 103528101 103529673 TCF7L2 GTRD no Colon (HCT116) 21642741
chr14 103528114 103529796 TCF7L2 GTRD no Colon (HCT116) 21642742
chr14 103528118 103530977 ZNF143 GTRD no Epithelial (MCF-7) 21642743
chr14 103528161 103529517 ZNF143 GTRD no Epithelial (MCF-7) 21642744
chr14 103528229 103530022 ZNF143 GTRD no Epithelial (MCF-7) 21642745

Genes associated with rs35382723[chr14:103528244], 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
chr14 103398716 103523799 - CDC42BPB ENSG00000198752.5 103523799 4445 Esophagus 0.0765533 13661