Tag | Content |
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EnhancerAtlas ID | HS118-17343 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:73993560-73996190 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:73993731-73993746 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr7:73995569-73995584 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34154 | chr7:73993814-73998430 | HCC1954 |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I074578 | chr7 | 73992698 | 73993671 | GH07I074579 | chr7 | 73993782 | 73996806 |
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Enhancer Sequence | GGATGAGGTC AAGGCTGCAG TGAGCTAGGA TCGCACTACT GCATGGGTGA CAAAATGAGA 60 CTACATCTCT AAAAAAAAAT TTTTTTTGAA AAGGAAGAGG AAGAAGGCCA GGCGCAGTGG 120 CTCATGCCTG TAATCCCAGC ACTTTGGGAG ACCGAGGCAG GCGGATCACC TGAGGTCAGG 180 AGTTCAAGAC CAGCCTGACC AACATGATGA AACCCCGTCT CTACTAAAAA TACAAAAATT 240 AGCCAAGCGT GGTGGCTCGT GCCGGTAGTC TCAGCTACTT AGGAGGCTAA GGCAGGAGAA 300 TTGCTGGAAC CTGGGAGGCG GAGGTTGCAG TGAGCCCAGA TCACGCCACC GCACTCCACC 360 CTGAGCGACA GAGCAAGACT CCATCTTAAG AAAAAAAAAA AAAAACTACA GTTCCCTTTG 420 TAAAATGGGT TTTTGGTAGA GACAGTGTCT TGCTGTCATT CCGGCTAGAG TCCAGTAGCT 480 GGGACTACAG GTGTGGGCCA CCATGCCCAG CTAATTTTTC CATTTTTATA GAGATGGGAT 540 CTTGCTATGT TGCCCAGGCT ACATTTTTTT TTAAATCATG AGTTTTTGAA GGAAATTGGA 600 TAGGGCAGGC TGTGGTAGGG GATGGATTGG ACAAGCCCCT GCTTGAATGC CTGCATACAG 660 TGGGGAAAAG GGGGATCAAA ATGGGTCAAG CCTTAAGGGT CCCTCCTGCA CGCAGTGTCC 720 AGGTGCAGGT CTGGGATGGC AGAAGAACCA CAGGCTCATG AGCACTGGCC TGGGCACAGG 780 TCCACAGGTC TCTGCCCCGC TGCAGCTTGG CCCTCCTCTC TCCAGGCCTC AGTTATCTCA 840 TCCATGAAAT GGAGCTGATG GAATTCCTGC TAAACCTGTG CACAGGCCCT ACAAGGGGTT 900 AAAAGCTGAA CCTGAATGTA GCTTTTTTAT TTTTTCGAGA CCGGGTCTCA CTCTGTCACC 960 CAGGCTGGAA TGCAGTGGTG CAATCGCTGC AGCCGTGAAC TCTGCCCGGG CCTGGCAGGG 1020 AGTTGGGGCT CTGTGAAGTG GTTCAGGAGG GGAGAGAAGG ACCATTATCC CACGCTTCTG 1080 CTACAGATCG CAGTCTCTCC CCTCTAAACC GCCCTTGCCC TTCGCTGGCT GCGTCTCCCT 1140 GCTGTGAATG GTCGTAATTA CCAACGTGAG GTCGTCAGTC TGAGCTGAAG TCCTCTAACT 1200 AGGCGGGGAG AGTCAGGGCT GGCCAGGGCT CTTGCACTTT GCCCCGAGAG AGAGCCGTGG 1260 AGCCAGCCCA GGCACCACCC GAGCCAGTTG GTTTAAAATT GTGTACATAG CATGGCTGTG 1320 ATTCAGTGAG CTTGGTTGTC TTTTTTTTTT CCCCCTTGGC AAATTTCAGT TACTCCTTGG 1380 GCTAACAGAC AGCAGACTGG TAAAGATAAG ATGAGAGTTG CCCAGCCAGC GTTAAAGAGA 1440 GAGAGGAGAC CGAAGAACAG AATGAGCAGG AGGGGGGCAG GAAAAATGTC AAGGGAAGGC 1500 CTGTCCACCA AAGGTGTCAC TGTCCAGGGG CAGTGGGCAG GAGGTCGCTG CTGCGGGGAT 1560 GGGTTCTTTC AGCAGGACTT TCTGCACAGC ACTGGGGGCA GAAACATGAA GGTGAAACCC 1620 TACACACACT GAGTCCTAAC TATGACATTT CCAAACAGAG AACACTCTGA AATGTTTGCA 1680 ACTGTGGGTG TCTTTACAGC CAGCCTGGGT TCAGGGGAGC TCAGGCAGGT CCTCCCGAGA 1740 ATAGGTTTGC TGACTTGGTG TTCCGGACGG TAAACTAAAC CCCCTTTTCT GGGGGGGGTT 1800 GGGGGGAGAC GGAGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCAGTGGCG CCATCTCGGC 1860 TCACTGCAAC CTCCGCCTCC CGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCCAAGTAGC 1920 TGGGATTACA GGCACCCGCC ACTATGCCCG GCTAATTTTT TTTTATTAGT AGTAGAGATG 1980 AGGTTTCACC ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTCAGCTGA TCCACCCACA 2040 TTGGCCTCTC AAAGTGTTGG GATGAAAGGC ATGAGCCACC GCATGCCCGG CCCATTGCTG 2100 CTTTACAGAT GAGGACATCG AGTGGTTCAG GGACTTGCCC AGGGTCGCGA GCTGATTGCA 2160 GAGCTGGGAT TTGAACCCAG GCAATCAGTC TTGGGTAGAC CACTGGGCTT GTGACCCTGG 2220 CCTTGAAGGG CCCGGTATTG CTCCTGCCCC TGCAGTGTCC TCAGCAGCTC TCTGAGGCGA 2280 TTCTCTGATC CGTGTTTTTC CCGTGAGCAG ATTAGACTCA AAGGTGACCG GGCATGCTGG 2340 AGCTGCCCTG CCCCACCTGA GGCCGAGGCC ACCACTGCCC ACAGCAGTCC TTGGGGAACT 2400 CCCTGGTGGC GACCTGGTGG TGGTGGCAGG AGCCTGGCTC TGTTGGGAAA GAGGACTCAT 2460 GACCCCACCT GCAGCTCTCC GAGATGCTCA GCTGGTCTGG GCACGATGGC TCACGCCTGT 2520 ATCTCAGCAC TTTGGAAGGC CAAGGTGGGT GGATTGCTTG AGCTTAGGAG TTGAAGACCA 2580 GCCTGGGCAA CATAGTGAGA CCTTGTCTCT ACAAATAACA CAAAAATTAG 2630
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