Enhancers that regulate TRIM27[ENSG00000204713.6]
Back to top
Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr6 28803095 28809375 enh90369 28891766 82391
chr6 28805076 28805418 vista51484 28891766 86348
chr6 28814625 28818775 enh91680 28891766 72991
chr6 28822567 28822754 vista51485 28891766 69012
chr6 28828749 28855295 enh49071 28891766 36471
chr6 28834475 28834586 vista51486 28891766 57180
chr6 28857185 28869275 enh9025 28891766 22491
chr6 28860175 28860528 vista51487 28891766 31238
chr6 28885422 28885544 vista51488 28891766 6222
chr6 28912265 28924255 enh57933 28891766 20499
chr6 28926865 28931015 enh91681 28891766 35099
chr6 28943532 28958995 enh59605 28891766 51766
chr6 28956602 28956848 vista51489 28891766 64836
chr6 28980530 28987543 enh90370 28891766 88764
chr6 28985048 28985267 vista51490 28891766 93282

Transcript facotrs that regulate TRIM27[ENSG00000204713.6]
Back to top
Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr6 28679868 rs1539586 G C 190911 Esophagus 0.0239789 8936902
chr6 28917091 rs9257404 T C 25325 Heart 0.00812454 8939087
chr6 29260431 rs3117425 C T 368665 Pancreas 0.0940669 8939730
chr6 29476675 rs116019240 C T 584909 Uterus 0.233558 8940007
chr6 28613079 rs139614182 T A,C 257700 Liver 0.357834 8936469

Genomic Location chr6:28870779-28891766[-]
TSS 28891766
Gene Name TRIM27
Ensembl ID ENSG00000204713.6
ENTREZID 5987
Uniprot
P14373
Protein Name
Zinc finger protein RFP