EnhancerDB
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Enhancers that regulate HMGCR[ENSG00000113161.11]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr5 74554625 74563675 enh55330 74632154 68479
Brain (SK-N-MC) Large Intestine
chr5 74569688 74575995 enh22364 74632154 56159
Placenta Neural Stem Cells (H9) Large Intestine
chr5 74612985 74623335 enh37983 74632154 8819
Bone Marrow (K562) Skin (Keratinocyte) Prostate (PC-3) Liver (HepG2) Cervix (HeLa-S3) Prostate (RWPE1) Esophagus Astrocyte Bone (Osteoblast) Stomach Colon (HCT116) Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Neural Stem Cells (H9) Epithelial (MCF-7)
chr5 74616844 74617109 vista48068 74632154 15045
VISTA
chr5 74656852 74664095 enh71804 74632154 24698
Thyroid Neural Stem Cells (H9)
chr5 74697442 74704443 enh59496 74632154 65288
Skin (Keratinocyte) Colon (HCT116) Lung (PC-9)
chr5 74732085 74738190 enh8501 74632154 99931
Blood (Karpas-422)
Transcript facotrs that regulate HMGCR[ENSG00000113161.11]
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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 HMGCR[ENSG00000113161.11], 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
chr5 73670595 rs11959706 T C 961559 Esophagus 0.127629 8308922
chr5 74141563 rs13180149 T C 490591 Esophagus 0.183483 8312124
chr5 74332066 rs62369187 A C 300088 Esophagus 0.352964 8313351
chr5 75121644 rs6870593 C G 463715 Uterus 0.471685 8315473
Details of HMGCR[ENSG00000113161.11]
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Genomic Location chr5:74632154-74657929[+]
TSS 74632154
Gene Name HMGCR
Ensembl ID ENSG00000113161.11
ENTREZID 3156
Uniprot
P04035
A0A024RAP2
Protein Name
3-hydroxy-3-methylglutaryl coenzyme A reductase
3-hydroxy-3-methylglutaryl-coenzyme A reductase
Alternative protein HMGCR
Expression levels of HMGCR[ENSG00000113161.11]
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