Tag | Content |
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EnhancerAtlas ID | HS118-06244 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr14:106362800-106364460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr14:106363231-106363246 | TGAACTTTGTCCTTG | - | 6.22 | Hnf4a | MA0114.3 | chr14:106363229-106363245 | ACTGAACTTTGTCCTT | - | 6.03 | RREB1 | MA0073.1 | chr14:106363665-106363685 | GGTGGGGTGGTGTTTGGCGG | - | 6.91 | TFAP4 | MA0691.1 | chr14:106363083-106363093 | ATCAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_13720 | chr14:106363972-106364703 | CD34_Primary_RO01536 |
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| Number: 2 | ID | Chromosome | Start | End |
GH14I105897 | chr14 | 106363021 | 106363090 | GH14I105898 | chr14 | 106363973 | 106364703 |
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Enhancer Sequence | ATTTTCCTTG TAGTTTTTCC AGGGGAAAGT TTATCCCTTA AGAAGACAGT TCATTTTGCC 60 TGGTGTAAAT TTTATTTAGA AGAAATCACA TTAAAAGTAT TTTTTGGGCT TTCCTCTGTT 120 ACTCCAATTA CTCAGCATTG TCATGAACTC AACCGCAAAG CCGCCTGTAG CCCTCTACTG 180 TTGTCCCCTG GCTGTCTGGG TTTGCATTGC ATGAACCTAC CATTGCTTAT TTGACTGTTC 240 TTCAGATGGA CGTTTGCTCT GTTCTCAGTT TGAGTCTATG ATAATCAGCT GTTCTGCACA 300 TCTTTCCCCA TGACGCTCTC AGGGAGGGCT CTGGGGCTGG CATTGCCTGA GGGTTCTGCT 360 TTGTCGCAGG GAGATCCTGC CAGGGCTTTT CAGAGTGTCT GTGCCCAGCA GCAATGCCTG 420 AAGGTGCCCA CTGAACTTTG TCCTTGCATC AGGCACTTTC TGTGTGTTTG CTTCTGTACT 480 GCTCCACATT CTGGAGAGTT TATTCAGATC TATGCTGCAA ATTCATCTCA CTGATTCTCT 540 CTTTAGCTGT GTCTACATCA GCTCTTAAGC ATCCCATGAT GCAATAGTGT GGTCACAAGG 600 CAAACTTTTG AAAGATGACA GTGTAGGATA GCGGCTGCTC CTCCTTCCCT GTGCTCTTCC 660 CACAGACTGC CCTCCTGGGC TCATTCCCAG CCACTGATCT TGAACACCAG TTTATGGAAC 720 TCTCTGCACA GGAAAGCAGA AACAGCAAAA GGCCCTGCTC AGGCTCTGCC TGCATCCCCT 780 CTTGCACACC TGCCAAAGCT CTTTCCTTGG GGCCTGTGCA AGCTTCCCAG AGCCTCTCAT 840 TTTCTGTTTA CCCTGCTCGC TGGCTGGTGG GGTGGTGTTT GGCGGGGAGT CTGGTGCATT 900 TTGGACATTG ATAGACACCC CTGGACCCTA CTTCCCAGAC GCTCCCCCAG CCCCTCAGCC 960 CCAGGAGTGG GTGTGTTTGC AGTAGGGCTT TGGGAATGGG TCTGTGTCAC TGTGGGAGTA 1020 GCAGCTACCA CCACTACAAT ATCCTCACAG TGACACGAGC CCCCACAAAA TCCTCCTGTC 1080 CCTACTGGTG TCACCGAGGT CCCTTTTGCT GGCTTTGGTC TGTTCTCCTG CTGAGACTGT 1140 GCATTCCAGC GGGTTGTTGT CTGAAACTCA GGGTGTCTCA GAGAGGACTC TGAGCCCAGT 1200 GCTGTATAGG GGGCTCCTCC TTTGTCCTGG GGGAGTTGCG TGGACCCTGT TTTTGGTCAA 1260 GGGAAGCATT TGATGGTGAA GGAGATCTCC CCTCCTCTCT TTCTCGGGAG CCCCCTCTGA 1320 TACTGTTGCC TGGTGTTTCT TGGGGCTGGT GCTGGGGGCT CAGCAGTCTC TGCCCTGTTC 1380 CAGGTGGGGC TGTGGGTGTG TTATGTTTCC TAGGTGTGTT ATGGGGCCAC CATTGAGGAG 1440 CTCGGGATGT CAGCGGCTGG TCTCTGTCCC TATGGTATGG GCTCCGGCTC ACTGCTCCCC 1500 TGCCCTCCAG GTCGGTCATT GACTCAGTTA CTATCCAGCA GCCTCTGTGG CTGTTTGGTG 1560 GTGGCTGCAG GTCTCTTCCC AGGAGAGGCC TGTGAGAGGA CTGGGATGTC TGGGAGCCCT 1620 GCATTCTCCC GTGATGCTGC TGCCTGGATC CCTTGTCTTT 1660
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