EnhancerDB
  1. Home
  2. SNP
  3. rs190110786[chr14:77483791]
Enhancers that have rs190110786[chr14:77483791]
Back to top
Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 77458104 77493935 enh3336
Colon (HCT116) Blood (Karpas-422) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Skin (Keratinocyte) Brain (SK-N-SH) Bone (Osteoblast) Thyroid Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs190110786[chr14:77483791]
Back to top
Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77483506 77484445 ZNF274 GTRD no Cervix (HeLa-S3) 21632173
chr14 77483778 77483793 MEF2C JASPAR yes 116720511
chr14 77483779 77483794 MEF2A JASPAR yes 116720512
chr14 77483780 77483792 MEF2A JASPAR yes 116720513
chr14 77483780 77483792 MEF2B JASPAR yes 116720514
chr14 77483780 77483792 MEF2D JASPAR yes 116720515
chr14 77483781 77483791 MEF2A JASPAR yes 116720516
chr14 77483787 77483798 FOXB1 JASPAR yes 116720517
chr14 77483788 77483796 FOXL1 JASPAR yes 116720518
chr14 77483789 77483799 MEF2A JASPAR yes 116720519
chr14 77483790 77483798 FOXL1 JASPAR yes 116720520
Genes associated with rs190110786[chr14:77483791], comfirmed by eQTL
Back to top
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