EnhancerDB
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Enhancers that regulate MED19[ENSG00000156603.10]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr11 57394745 57399915 enh13936 57479693 79778
Placenta
chr11 57403151 57414495 enh13937 57479693 65198
Brain (SK-N-SH) Prostate (RWPE1) Bone (Osteoblast) Placenta Peripheral Blood (MM.1S) Uterus Heart
chr11 57406709 57407290 vista10357 57479693 72403
VISTA
chr11 57439825 57445563 enh62158 57479693 34130
Esophagus Stomach Thyroid Lung (PC-9) Neural Stem Cells (H9) Epithelial (MCF-7)
chr11 57486005 57490155 enh74810 57479693 6312
Muscle (A673)
chr11 57494357 57503795 enh1785 57479693 14664
Blood (OCI-LY7) Colon (HCT116) Blood (Karpas-422) Lung (PC-9) Neural Stem Cells (H9) Epithelial (MCF-7)
chr11 57527165 57531315 enh98815 57479693 47472
Uterus
chr11 57536385 57549074 enh13938 57479693 56692
Astrocyte Colon (HCT116) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Kidney Stomach Skin (Keratinocyte) Brain (SK-N-SH) Ovary Bone (Osteoblast) Lung (A549) Thyroid Pancreas (Panc1) Neural Stem Cells (H9) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Prostate (RWPE1) Lung Muscle (A673) Heart
chr11 57542885 57543297 vista10358 57479693 63192
VISTA
chr11 57546018 57546724 vista10359 57479693 66325
VISTA
chr11 57549936 57550183 vista10360 57479693 70243
VISTA
chr11 57551945 57558455 enh13939 57479693 72252
Esophagus Astrocyte Blood (GM12878) Muscle (A673) Placenta Neural Stem Cells (H9)
chr11 57559748 57559971 vista10361 57479693 80055
VISTA
chr11 57564288 57569075 enh1786 57479693 84595
Bone Marrow (K562) Liver Astrocyte Adrenal Blood (Karpas-422) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Thyroid Neural Stem Cells (H9) Prostate (PC-3) Large Intestine Esophagus Placenta Lung (PC-9) Breast Liver (HepG2) Prostate (RWPE1) Heart
Transcript facotrs that regulate MED19[ENSG00000156603.10]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
SNPs associated with MED19[ENSG00000156603.10], confirmed by eQTL
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Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr11 57566850 rs483030 A G 87157 Esophagus 8.57054e-10 2010623
chr11 57480623 rs576859 C A,G 930 Esophagus 3.37063e-09 2010198
chr11 57479731 rs141274831 CG C 38 Breast 0.000106615 2010182
chr11 57479731 rs141274831 CG C 38 Uterus 0.221335 2010182
chr11 57538894 rs199510392 T TTATATAGAG 59201 Lung 1.21441e-08 2010443
chr11 57529130 rs558653 C T 49437 Stomach 3.49851e-06 2010393
Details of MED19[ENSG00000156603.10]
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Genomic Location chr11:57471186-57479693[-]
TSS 57479693
Gene Name MED19
Ensembl ID ENSG00000156603.10
ENTREZID 219541
Uniprot
A0JLT2
Protein Name
Mediator of RNA polymerase II transcription subunit 19
Expression levels of MED19[ENSG00000156603.10]
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