Tag | Content |
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EnhancerAtlas ID | HS118-05634 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr13:114739920-114741400 |
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) |
INSM1 | MA0155.1 | chr13:114741304-114741316 | TGTCTGGGGGCA | + | 6.44 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_00138 | chr13:114739755-114742997 | Adipose_Nuclei | SE_32419 | chr13:114739890-114742608 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113970 | chr13 | 114739950 | 114741168 |
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Enhancer Sequence | NNNNNNNNNN NNNNNNNNNN NNNNNNNNCG GACCTCTTGA AACTCCTCTT TGTCCTAGCA 60 CAGCTGGCTG GAGGTAGCTG AGCGGGAGGG TGGGAGAAGC CCACAAGACC TGCCCATGCC 120 GGCTACTACC CCCAACCCAG GCTTCCTCTC ACGGACAGGT GGGACTTGAA ACCCCACTTG 180 GCTTGTCCAG GAAAATCCAC CAATCCCCAG GGTCTCTGGG CTCCCCGAGA GGCATTGCGG 240 GATGTTTCTA GCAGTCTTTT TTCGGGACCA CTTTATGTCT CGTGAGGATC TTTACCTTGA 300 TGTGACAGAG GACAGGGGCC CAGGAACATC AACTCGGGTG AGCGGTGCTC TGGTGCTCCC 360 GGCAGGAACC CAAGCCTGGC TGTTGGCCAC CGGCTTGCAC CGAGCACACA CTGCTCCCTG 420 GCACACTTGG CTAAAGGTGT TGACTGACTT GGCCAACGTG AAACATTCCA TTCTAGTTAA 480 ACACTGAGTT CTCCGTTCCC AGGAGCTTGC AAACCAGCAC AGCCTTGTGA GGAAGTCATG 540 TGGCAGAGGA TTCTCCAAGC CCTAGGTGCT CAGGAGAGCC TTGGAGTGAG CGGATTCCAG 600 ATCCCACAGG GCCTCCAGCC GCATCGGAGC CGGGAATGTT TGCGGAGACC CTGGCTTCCC 660 GCAGCTACTC CCTCTTCCCA CAACACCCCC TTGGCCCGGG ATTCAAATAC AACAGGGATG 720 ATTCCAAAGC TTTAAATGAT GCTTGTGATG GAAGAGACCA GACCTCCTCC CAGAGCTCGG 780 CAGAGTCACA TGGGCCACTC CAGGCAGGTC ACTCAGCTCA GCCCACAGGC CCAAGGGGCA 840 GCTGGGGAAT GGGGCTCTTC CAGGGAAATG AGACCAATGG CCGACCACGA GGGGCTGCCC 900 CCAACAGAGA AGCCACGAGT GGGGCCCAGA GGTGGAGCGC AGAGCCTTTG CAGAATCAAC 960 AGGCGTCCAG GGTGCATGTG GGCTCAAGGC AGGGCCTCAG TGGGTCTGGA ACCCAGCGGA 1020 TTCTCACTGT GCTCTTGCCG GCCTCTCTGG GCTGCCCTCC GTGAGCGCTG GTCTCCTGTG 1080 CTCCGCATGG CCCAGGCCCA GACACACCCC ACTGGTGCCC CCGTGAAGTC GGCCACCCCA 1140 CGTCTCCCGC ATCCCGGAGG CCTCCCTGTG AAGTGGACGC GGCGTCTCAC ACATCCGGGC 1200 ACCTGTGGGT GCACGTGGCA CTGGGCATGT CATGGAGCCC ACCAAGTCTG CGAGGGGTGA 1260 GGAGCTGAGT CCCTGCAGAA ACCAAGGCCA CGTCGGACTC TACCAGTGGT CAGCAAGGCC 1320 CGGCCCTTCT CCTCGGGTCA CAGGGCTGGA AATGCCTCCT GCTCTTCTCC GGCAGAATCT 1380 CAGTTGTCTG GGGGCAGCCA CAAAGCTCCA GGGAGGATGC GCTCCTGGGC CGTGGTCTCG 1440 AACCCTGAGG GTGCTGGTGC CTGGGGGAGG CTGTGCAGGG 1480
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