Tag | Content |
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EnhancerAtlas ID | HS091-06159 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:101117410-101119750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:101119639-101119660 | AAAGCAAAAGAGAAAGAACCA | - | 6.25 | TBXT | MA0009.2 | chr10:101118828-101118844 | TCACACTAAGGTGTTA | + | 6.38 | TBXT | MA0009.2 | chr10:101118828-101118844 | TCACACTAAGGTGTTA | - | 6.7 | ZNF263 | MA0528.1 | chr10:101118505-101118526 | TCCTCTCCCTCCCCCACCTCT | - | 6.84 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I099358 | chr10 | 101118001 | 101118170 |
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Enhancer Sequence | CAGTAAGTGC ACGGCCTTGG CTGTTCTCCA GGGTCATCTT ATTTTCCTCC AAGACTCTCA 60 GGTAAAGCCT CATTTGATTT ATAGAAAGGG TGTCAGGGCA AACCCTGTGC CCTGATGTGT 120 GTCAGCCACC TATGCCAGGT GCTGCTGTGG CAAGATACCC TAGTTGGAAT CACTTCTGAG 180 TCACTGGGAA CATGCTAGCT AAGTGTTTAT CAGGAGGGAA CCTTCAGGAA CTGAGCCAAG 240 ACTATGAAAA GGAGACCTCC CAGCCTTTGG ATAGAAACGG GACTACAGGA AACACAGTGT 300 TCCCAGGACG GTGCCCAGAG GCCTCTCTGC CCTTGTTTCT GTCCCCTGTG TTCTTGTTTG 360 GTTGCTTCAT CCACCTAGAT GCAGACCCCA ACAGGGGTTC CACTCACATC AGAACATCGC 420 AGTGAGCAGT GGAGACTGTC ATGAGATTGC CTACTCACAG CCTAAGCCAA AAACTGAATA 480 CTCCTTCTTA CAAACTTCCC TGTCCTCTTC TGCCTTTCAG CCCACCACCC TGGGTTTCTG 540 TTCTCTCCCT GCCACCAGCA TCCCTGCTCT TGTCTCTGCT TCCTTCTTTC TGGTCTGCTG 600 CCCCTCCTAA CTCCCTCACT CAGGAACAAT ACAGACTTTT CTATGCAGAT GTGAGTACTT 660 TGGGTTACTG AACCTTATCA AAGCTTTGCT TGCAAACATT ACAAAGGCAT GCTTTGTCTT 720 TAGGATTGGA ATGTTATCTA AGTCCATGGG AGTCCCTAGG CTGGGAAGTG TTTCCTCCTG 780 AGAATTTCAT CTCATGGAAT AGCCATCCTT TTCTTCCTTG CAGATAACTC GTTTCAGACT 840 TTGGTCCTTA GTTTGTGAGA TGCGGCCTTT CAGAAACTGG CTCCTGGTAG AAAGAGCTTT 900 GATACCATAA GGCAGTGAGC AGTGCAGAAA GAGTGCCTTC CTTTTAGACA AAGAAGAGAT 960 CAACTCTAAA AGGTGGGCCA GGCCTTGGCA AAGACAAGCA AGAGAGTCAT GGCACCTCCC 1020 TCCAAGAGCC TGGGCACTGC TGTGCTTGCC CGGACCAGGC GTGTCTTCCT CACATGAGGA 1080 ACGAGCTCGG AAATGTCCTC TCCCTCCCCC ACCTCTGCCT GCCACTCTTG ATTTAGAATT 1140 CTCAGGTGTA GCCTGGGCAA CATGGTGAAA CCCCATCTCT ACAAAAAATA CAACAGTTAG 1200 CCAGGCGTGG TGACGTGTGC CTGTAGTCCC AGCTACTTGA GAGGCCAAGG TGGGAGGATC 1260 ACTTGAGCCT GGGAGGTCCT GGCTGCAGTG AGTGGAGATT GTGCCACAGC ACTCCAGCAT 1320 GGGAGCCTGG GTGACAGGGC AAGACTGTCT CAAAAAAAAA AAAAAAAAAA AAAAAAAAAA 1380 AAAAATCCCA GGTGTCTCAG ATAAACTAGT GAAGCCATTC ACACTAAGGT GTTAGGTACT 1440 GATAATAGTC TAAATGAGTA AGCTCCTCCC AGGGCACTTG TTTGAACAAC CTTAAGGCTT 1500 CCAACACACA CTATTGAAAT CTAAGGAGAA GGGGGCGATG AGAGGAATGA TTTCCTAATA 1560 ATGCCATGTT AAGTGGCAAT CTGATGGGGG AGAGGGGGGC TATTTAGGCA AACTTATCAT 1620 ACAAATCAGA AAGTTGCTCA CTAGTGAGAG CGAAAGAGCT GGGCTAATAG CCTGTATTTT 1680 GCTACTCTTT TGCTGAGTGA TCCTCTTTCT ACAGGAGCAG GTTAGGGTCT TTCTACCTAT 1740 AAATAGCTGC TGGCATGATT CCCTAAGAGC TATGAAAAGG CCCAGAAGCC AGGGATACTG 1800 TCTTTCTTCT TGCATGACCC TGACCTCTTA CGTGATCTGG ACACCTGGGT CTGGGTCTGC 1860 CCATTGTGAC TTGAGCAAAA GGAGTGTCAA AGCAGGGGCC AGATGACTGT GAAGGCCCAG 1920 AGTCAGAGCG GGCCATGGAA GAGCTGCACC GGCAGGAGGG CACTTTGACC CTTCTAGAAG 1980 GAAACCCAAA AGCAGGCCCC AAAAGGAGAG GGGGCACACC AGGGAGCCGG ATTCTGGGGC 2040 CTTATTTTCC TGCCACAGGG GTTCATTCCC TTTCATTCTC ACTGCATCCA CTCAGCTTGC 2100 ACCAGACGTT CCCCCACAGC CCTGTTTCTC TTTAGGCGAA GTTTGGAGAA AACCCAAATC 2160 CCTCTCCCTG TTCCCCTTAG TGCAGGTAAG ATGGGCTAGC AGTTTCAAAA TTTTACTCAA 2220 AACTCAGGGA AAGCAAAAGA GAAAGAACCA AAGAAAACAT TTCCTCTACC AAAAAAAAAA 2280 AAACAAAAAA AAAAGCGGGG GCCGGGGGGG AAGTAGATAT ATTTAGACAA GCTTTAAAAA 2340
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