EnhancerDB
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Enhancers that have rs140119459[chr14:100415787]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 100408665 100423755 enh15933
Cervix (HeLa-S3) Large Intestine Esophagus Liver Placenta Colon (HCT116) Pancreas Muscle (Myotube) Uterus
chr14 100415478 100415881 vista19073
VISTA
Transcript factors that have rs140119459[chr14:100415787]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 100414921 100418270 ZNF274 GTRD no Cervix (HeLa-S3) 21638322
chr14 100414921 100418270 ZNF274 GTRD no Cervix (HeLa-S3) 108122817
chr14 100415243 100418017 ZNF274 GTRD no Cervix (HeLa-S3) 21638323
chr14 100415243 100418017 ZNF274 GTRD no Cervix (HeLa-S3) 108122818
chr14 100415328 100418010 ZNF274 GTRD no Cervix (HeLa-S3) 21638324
chr14 100415328 100418010 ZNF274 GTRD no Cervix (HeLa-S3) 108122819
chr14 100415525 100418121 ZNF274 GTRD no Cervix (HeLa-S3) 21638325
chr14 100415525 100418121 ZNF274 GTRD no Cervix (HeLa-S3) 108122820
chr14 100415539 100418117 ZNF274 GTRD no Cervix (HeLa-S3) 21638326
chr14 100415539 100418117 ZNF274 GTRD no Cervix (HeLa-S3) 108122821
chr14 100415570 100415975 STAT3 UCSC Txn Factor no Conserved 108122822
chr14 100415612 100416912 ZNF274 GTRD no Cervix (HeLa-S3) 21638327
chr14 100415612 100416912 ZNF274 GTRD no Cervix (HeLa-S3) 108122823
chr14 100415612 100417941 ZNF274 GTRD no Cervix (HeLa-S3) 21638328
chr14 100415612 100417941 ZNF274 GTRD no Cervix (HeLa-S3) 108122824
chr14 100415631 100416649 ZNF274 GTRD no Cervix (HeLa-S3) 21638329
chr14 100415631 100416649 ZNF274 GTRD no Cervix (HeLa-S3) 108122825
chr14 100415752 100416249 ZNF274 GTRD no Bone Marrow (K562) 108122826
chr14 100415783 100418016 ZNF274 GTRD no Cervix (HeLa-S3) 21638330
chr14 100415783 100418016 ZNF274 GTRD no Cervix (HeLa-S3) 108122827
chr14 100415786 100415795 SP1 TRANSFAC yes 107610229
chr14 100415786 100415795 SP1 TRANSFAC yes 117744141
chr14 100415787 100415797 SP1 JASPAR yes 107610230
chr14 100415787 100415797 SP1 JASPAR yes 117744142
Genes associated with rs140119459[chr14:100415787], 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