Tag | Content |
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EnhancerAtlas ID | HS118-07484 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr16:72910710-72913100 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr16:72910889-72910899 | CCCAATTAGC | + | 6.02 | NFYA | MA0060.3 | chr16:72912299-72912310 | GGCCAATCAGA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37618 | chr16:72908384-72913399 | HSMMtube |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I072872 | chr16 | 72906657 | 72914500 |
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Enhancer Sequence | CTCACACACG GCAGCCAGGT GTGGTTGAAA CATTCTTTCC AGATATCTAT GATATATGCC 60 AACATCCTTC CCTCTGGGGG TCTTTCAACG TGAGCCTGAC AATCCCAAGG GGAACAGAGA 120 CTTGGCGGGG GAGAAAGGGG GGTGATTCCA AAATAGTTAT TGAAAAAGAA TCACTATTTC 180 CCAATTAGCC CTGTAATAAT GCCTTACAGG AATGACTGGA TGCCCTGCCC CTGCACGCCA 240 TCTACCAAAA CCAAAAAATA GTCTACATTC CTGATTAAAG CAAAGCTCAG AGAAAACAGC 300 CCGGTATGGC ACAAATCTCC CCGGTCTTAT GTGTTCTGAG GAAGTCTTCA GATCCGCCCA 360 GGGTCTGGGC ACAGGTCCGC AGGGAATCAA ATGGCTGCAG AATTCGATCA GGCCTGTCTG 420 TCCAAGGCCA GCTAGATATG GAAATCAGAA GTAGGTCATC AGCCCTCAAG AATCGGATAA 480 TGACCTCTGG ACTCGCAGCG CTGGGGCCAC CAAGAGAACA AAGGTGTTAA GGCACTGTGT 540 AGGTTTTTCT GTTGTTGTTG TTGGTGTTGT TGTTACAATA TCTAATAGTG AGATCAAATT 600 CTTATTGTGG AAATAAACAT CACGGTCTTC TGTATGAAGA TGGTCTGCGG AAAGTGACCA 660 CGCATCAGAG TGTCCAGCGT AGGAGGAGAA TCTCAGTTTG CCTTAGTCAT CATAGCACAC 720 ACCCTGAGCA CAGTAAGTTT CTCATTCTTC GTGTCTGGTG TTTATGTTGT AGTAGAGACG 780 ACTCGTCCTC AAGTTAAAAG GACAAAAGTC TTTCCTGTGT TTCATACTTG GGCGGTGAGT 840 CACTAGGAAA GGATTTGGTT TTTAGAAAAA AAACTTCTGA TCCCTGGGCT AAAACAGAGA 900 GCCCCAAAGA GCTATGTTGA TCCCAGACAA GCACGTGCGT GGATTCTTCA AAGTTCAGGT 960 CAACTCAGGC CCCTCCTCCT TGCAGTCAGC CCTGTACTCA AGGTTGCTGG AGACATGGCG 1020 CCTCTATTTC CTGCCCAAAG AAGCCCCCTT AACTGGGGGC CACGGGTTGA GTGGTGAAGG 1080 AGGCAACTCA CACCTGAATT ATAGTGGGCT TGTAAACCTG AACAGGGCAA GTCACAACTT 1140 TGGGAGGCTG AGGCAGGAGG ATCACTTGAG GCCAGGAGTT CAAGAACAGC CCTGACAACA 1200 TAGTGAGACC CTGTCTACAA ATGAAAAAAC TAGCCAGGTG TGGTGGTGCA TGCCTGTGCT 1260 ACTTGGAAGA CTGAGGCAGG AGGATCACTT GAGCCCAGGA GATGGAGGCT ACAGTGAGCC 1320 ATGATTGTGC CACTGCACTC CAGCCTGTGT AAAGACCCTG TCTCTACAAA AAAAGAAAAC 1380 AAAAACAAAA ACAAAAAAAC AAAAAAAACT CACCTACCAA AAGTCCAGCT GACATCTACT 1440 ACAAAATTCC CATTATTGCC ATAAAAACAT GTGGGCTGGG TTCAAGGCTG CATAGCAGAT 1500 GGCCAGGCTA CATCCTCATC ACACACGCAC TTCACTGGTG CCAGTGCCGG TGACAGGCTA 1560 GAAGCCACTC CAGTGAGGAC CCCTGCCAGG GCCAATCAGA TCAGGGCTGC CCTCCCCATG 1620 CTGTGGGGCT TCTCAATGCT TCTGAAATGG ACTCACACAA GGAAGTCACA AAGGGCTTTG 1680 GACATTAGGA AAACCATGCA AACTGTTTCC ACTTCTCAGA GCAACCCGAG GCACGCGCTC 1740 TGGAGTGTGC AGAGTCACAG ATAACTGCTG CTGCTTTGCT CACCGCAGTC TTAGGATTTC 1800 TTCATTTCTA TCCTGGAGAG AATCCAGCAA TGGATCACAC TGTTATCTAG ACACAAAGAA 1860 TCCCACCCCT GGGGCAAAGT GCTACTTGTC CCGTGGATGA GTTTGTCAGC CTGCAGCAAG 1920 GAGGCCAGAC GCAGTGGGAA GAGCACAGCC CTGGGCCCTG GGCCTCTGTA CCAAGTCCCT 1980 ACTCTGCTGC TGTCTACAGC AGCCCTGTCC TCAGGAACCT TCTCCAGGGA AGGAAATGGC 2040 TTCTGTCTGC ACATCCAATA CAGCAGCCAC TAGCCACATG GCACTGAGAC AGATGGGCCG 2100 CTGCAATGGG AACCTAGCGA CATGAGACAT CCAAGATTGC CAGGAAGGGT CCGAGTTCGC 2160 CTCTGCTTTA TGCTCGTGCA GGACAGGAAC GGCCCTGTGG AGGCTGCCCT CGAGGCTCAC 2220 ATCACAGGCT CAATCTGGGA AAGACCAGCC ATGGGAAGCA GGATGTGACT TGCCCTGGAA 2280 GCGCAAGTGA AGGACGGGCT CCGAATGAAA GCTACACAAG GTAACAATAT ACACACTGGG 2340 ATCTTTATAT TATGTCCAGC CTGGAGTATA TAACACAGGG TAAGGAAAAA 2390
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