Tag | Content |
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EnhancerAtlas ID | HS118-16123 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:42219260-42220660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr6:42219747-42219757 | GCTAATTGGG | - | 6.02 | Gfi1b | MA0483.1 | chr6:42219382-42219393 | AAATCACAGCT | + | 6.14 | HSF1 | MA0486.2 | chr6:42220551-42220564 | TTCTAGAAGATTC | + | 6.57 | NR2C2 | MA0504.1 | chr6:42220526-42220541 | TGACCTCTGCCCTTT | - | 6.73 | TCF3 | MA0522.2 | chr6:42219549-42219559 | AGCAGGTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27413 | chr6:42219643-42220578 | Esophagus | SE_33893 | chr6:42219039-42220940 | HCC1954 | SE_53138 | chr6:42219398-42220741 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I042250 | chr6 | 42217780 | 42221554 |
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Enhancer Sequence | GCAATTTTTT TTTTTTTAAT TTAAACCAGT GCCATGTTAG GCAAGGTAAA AGAGTATTAA 60 CTCAGTACTG CCCTTGAGGG GACCACTGTC TAGAGACATA GGCTAAGGAT GCCTGGAAAA 120 TGAAATCACA GCTGTGCTTC TTGCAAATTA CTCTCTTGAG TACGTAATTC TGTCTCCTCA 180 TCTAACTGGG GCAGCTTCCA AGGCAGAAGA GACAAGGCCT CTCCAATGGA ATGAGTATTT 240 CCTCCAGGTC TCCTCCATCT CCACAACTCA GGTCAGGGTT TCAGGACTAA GCAGGTGTTT 300 GGGCTGTGCT CAGGGCCAAT AAGTAGTCTC AGCTGAACAC TTGCCAAGAA GCCAGGTCAG 360 TTCTAACACC CCTCTGCAGG AATGACCAGT TCAATGAAAA AAATCAAGCA TGCTGCAATC 420 CATCTAATCA CAACCAGGCT TCGTCTCCAC CCTGACTCCC CCATGCTTGG CCCTTCCCAA 480 CCCAAGTGCT AATTGGGAAC CACTGCACAC AACTGCTAAC CACACATGGG TGGGAAGGTG 540 CTGAGAGCAA CAGAGGGCTG GACTGTGCAT CGTGGTGGGG GTTGAGCGCC AGAAGCCACT 600 GCAACAGCAC TTTCCTCTGT GGATCCTGTA CAGGGTTCAT GTGGCCTTGG CAAGCAGCCA 660 TTAGATCTGG GCAAGTTGCC CACCACGTCG GCCCTTCCCC CATAGCACAT CTCTCCTGGG 720 TCCCAGCACT GGTCACTTTT TCCTTTTCTT AATGAACGGC TTGGAGTGGG TGGGAAAGGG 780 AAGATAATGA GTAAAGTAAG GAAGTGATTT TCGTAGGCCT GTGTCTTTGT CTTTCTCCCC 840 AAACTTACAG CCTCCCGCCC TGACATGGAC AGGCTCAGGC AGGCCTGGGA GACCTGAACT 900 CCCTCTCCAG ATAACTGGGA GCCTGGAGAG CAAATTCGGG GCTGGGACTC AGGATGGTGA 960 CACTGGCCAC AGCCACAGAG TCAGGAGCCA AAGGAGATCC AGAAGATAGG GTCCCAGCAA 1020 GGTGGCAATT AAGCCAACAG GCAGTCACTA CTGGGGAGCA ACCCAACAGG GCTCAGCACA 1080 AAGGCCAAAG CAGAATGGGG CCATGGAGAT GGGATTCACT GACACCTGGG AAGCAAATGA 1140 GGGGGTTCAG CAGTGGGAGA AGGAGGTGGT GGCTGGGACA TGTGATGGGG AAGATTCTGC 1200 TGCCTCCCCT GCGGCTTAGA AGGAAACTGT TAAGGAGATG GTTTTGGGTC AGACTTCAGA 1260 GACCAGTGAC CTCTGCCCTT TTTGCTCAAA CTTCTAGAAG ATTCTCTGAG TCCCAGTCTA 1320 TCATCACTTC CTGGAGAAGG CAAGTGACTG GCAAACATAG GTGAGTATGT TTCTCTTGGA 1380 GATATCAACC CTTCACAGCT 1400
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