EnhancerDB
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  3. rs7144969[chr14:103674349]
Enhancers that have rs7144969[chr14:103674349]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 103649674 103677715 enh15975
Bone Marrow (K562) Liver (HepG2) Cervix (HeLa-S3) Brain (SK-N-MC) Large Intestine Prostate (RWPE1) Esophagus Astrocyte Bone (Osteoblast) Stomach Placenta Uterus Embryonic Stem Cell Line (H1-hESC) Lung (PC-9) Pancreas Pancreas (Panc1) Neural Stem Cells (H9) Epithelial (MCF-7)
Transcript factors that have rs7144969[chr14:103674349]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 103673191 103674453 POLR2A UCSC Txn Factor no Conserved 108126701
chr14 103673778 103674688 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21643441
chr14 103673778 103674688 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108126715
chr14 103673871 103674531 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643447
chr14 103673871 103674531 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108126721
chr14 103674001 103674511 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643450
chr14 103674019 103674399 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21643451
chr14 103674346 103674362 NFYA JASPAR yes 117967629
chr14 103674349 103674364 NFYB JASPAR yes 117967630
Genes associated with rs7144969[chr14:103674349], 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