Tag | Content |
---|
EnhancerAtlas ID | HS091-37990 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:34033560-34035750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr5:34034098-34034113 | TTTACAAAAATAGAA | + | 6.23 | Nr2f6(var.2) | MA0728.1 | chr5:34034181-34034196 | TGACCTCTTGAGCCT | - | 6.4 | TCF7L2 | MA0523.1 | chr5:34034456-34034470 | TTTCTTTGAAGTTT | - | 6.2 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29386 | chr5:34033203-34036016 | Fetal_Intestine_Large |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I034033 | chr5 | 34033609 | 34035832 |
|
Enhancer Sequence | TTCCTTAAAC AACCAGACAT CATCACATGA GAAAACCCAG TCACTCATAC TTACCATCCA 60 TTTCTAGACA TACTATCCAA ACTCAATTAT GAAAGGGGAC CATTCAGAAT AATCCCAAAT 120 ATAACCAAGG GGTATCATCA TCTAAATAGG GCAATAGGCT CTGAAAGAAG CCTTAGATAC 180 CCTAAAGCTC CAAAGCCTGT TTATCCTTTG AAGCGAGGCT TGGAGGAAAA ATTGTGTACA 240 ATTCTGATTA TCACATTATC ATTTAAAATA GCAAAGATTG GAAACCACCT ATATAATCAC 300 CAATACTAGG AGGGCATGAC ATATTCTAGA AACTATGTTA TATAGTCATA AAAAAGAAGG 360 CTGAAGAAAA ACATTTAATG ATATAGTGAT ATTCATGATA TTTTTAGATT TTAAAGTTAT 420 AAGTGGCCAG GTACAGTGGC TCACAACTGT AATCTCAACA CTTTGCGAAG CCACAGTGGG 480 AGGATCACTT GAGCCCTAGA GTTTGAGACA AGCTTGAGCA ATATGGTGAG ATCCCATCTT 540 TACAAAAATA GAAATTAAAA AATTAGCCAG GAGTGGTGGT GCACACCTGT AGTCCCAGCT 600 ATTTGGGAGA CTGAGGCAGG ATGACCTCTT GAGCCTAAGA GGCCAAGGCT ACAGGGAGCC 660 TGGATCATGC CACTTCACTC CAGCCTGGAC AAAAGAGCCA GACTTTGTTT CAGGCAAAAG 720 AAAGTTATGA GTAAATAGAA ATAACATGAT ACTATCTTTG TTTGGAAAAA TATGTGTTTA 780 TGTATTATAT CCATAGGGAA AAAAAGACAA GAATAAGTTA CAGAAAAATA TTCACAGAGG 840 TTCTTTTCTA AATGTGGAAC ATGAGTAATT TTCATGTCAT TCTGTATATT TTTCTGTTTC 900 TTTGAAGTTT TCTACAAAAA ACACATCACT TTTATAACTG GGGAAAAGGT AAACTCATTC 960 ATTAAACAAA TTACAGCAAT GATTTTGAAA GCAAGAGTTG GAAAACAATT TTAACTTTTC 1020 CCTTTGCCAA CAAGAGACAA TTTCTACACC TCTTCTTTAT TTTTAATATT TGCTAAATTT 1080 CAGGCTTTTT GCTGTTCATT TTGCATGCTA CCCTTGGTTG GTTATCATAC CAGGCTTACA 1140 ACCCTACCAA ATGGATGAAC TTTGACTGTG TTTACAAATT AATGTGTTCA GTGACAAAGC 1200 CATTTCCTGG TTAGAAAACA TTTAACCAAG GCCAATCTTT TGTGTAACCT CACAAGAGTT 1260 AAGACCTGAG AAGATTTTAC AAGGGTCGAA GTAGGCCCTA CCCCTACATC ATTGCTCCTG 1320 CTGGCTGCTG TCCTTGATGG CCAATGACAT AGATTCCAAG CCAGTAAGTG TAGTTTAAAG 1380 TTTAACATAA GATTTTCTTG CTGTAAATTT GGTTTTGTGC AAGAAGCTAC TCAAAAGTAG 1440 AAAAAAAATT GAACCACATT TGATAAATAT TAACATCAAT GAGAGTAAGT CACAGAAGAG 1500 CCAGTGGACT TTGGCCAGAC CCTGAGATGA GGTCCTACCC TAGGGATTAA CCTGAGGATG 1560 AAGACAATAA AACCCAAGAT AGGCTTGGGA GCCCCATATT GAGGAGACCT GGGCTACCCT 1620 TTCCTGGACT GACCCAGGGT ACCAGCAGGC CCGCGGCACT CTCCTATGCC TGGTGGCATT 1680 GGCACAGTAC AGATGACTGA ATTGCTGGTC TAGTGGGGTC TCATGTAGCT CCAGAGCATT 1740 CCCCATACCA CTACATGGTA CTGGAGCCTA AAAATGTTTC CATGAGGTCA AGAGTGGCAT 1800 GAGAGTCAAC TGAGAGACGG CTGAACATGG AGAGATCCTG AGACTGGAGG AAGAAGCACT 1860 TAGCTGGACC TAGAGTCACA CAGAAGGATG CACAGCTCAG TGACTGGCAT TGAGATGGCT 1920 GTAGCCCAGA GCAGTAAGCT TTTGGCTCTA CTCTGCCCTT CATAAAGCAT GCTGTGGCAG 1980 ATATACTGGA ACGAAGACTA TGACCTGGTC GTTTCGGACT CAATGCTGTT GAGGAGCCTC 2040 CCAGCCTATG AACCTGGTAT TCCAGGGTGC CAAGAGTCTA GCGGATCCTT TGGATCACAC 2100 AGAAGTGATC CCAAATTATT AAGGTTTGCC CTTTGCTCCT ACTTTAGCTC AGGCTGCAAT 2160 TAGATTGACA GTATGTCTTG CTCATCCTTA 2190
|