Tag | Content |
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EnhancerAtlas ID | HS091-14608 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:42682300-42684830 |
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) |
HES2 | MA0616.2 | chr15:42684228-42684238 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr15:42684228-42684238 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr15:42684364-42684385 | AAAACAAAAAAGAAAGAAAAA | - | 6.46 | Nr2f6(var.2) | MA0728.1 | chr15:42683209-42683224 | TGAACTCCTGACCTC | - | 6.22 | SOX10 | MA0442.2 | chr15:42683423-42683434 | TTCTTTGTTTT | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28452 | chr15:42683246-42689681 | Fetal_Intestine | SE_29385 | chr15:42683334-42689647 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I042391 | chr15 | 42683482 | 42689512 |
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Enhancer Sequence | ACACCTCCGA TTATCAGAAC TGACCATCCC TCCAACCCAC ATGACCCCGC CCTATTAGTG 60 TCAGACTCCC CTCAGCAGCC AGGGCCTTAC CCACACACCC CCACCTGGCA CCTCCCAAGG 120 GTCTGGGTTG AAATAACTTG CTCAGCCAAG GCTCCTGAAG AGGGTGCAAG AACCAGGATT 180 TTGGAGGGAA TCTCTGCTGG AGTTTCTGCA TATTCCATGG TCCAGGCAGT TCCTCTCATA 240 ACGAACTATC AGACAGAAAT ACTTGTAAAG ATACTTCATT TATTTTGAAA TATTTTTCCT 300 CTTCTAATGT ATTCATTTAT TCATTCAACA CTTATTTTTG AGCTCCTACT ATGTTCCAGG 360 CACTCCTCTA GCAAACAAAG CAAATTCTCT CCTCTTTTTC AATATTTGTG GAAAAAGCAA 420 GGTCTCCCTC TTGTAGAGTT TATATTCTAG TATTTTCATA AGTTATACCT GCTCACTGGA 480 GAATACTGAG CCATACAGAA AAACACAGAG GAAAATTTCA CTTATATTTT TCCCCATGTA 540 AAGATAACCA CTCTTAACAT CTAGTATATG TTCTTCCAGG ATTTTTCTAT GCACACACTG 600 AATCTGTATT TTTATTTTTA AAATGTTATC ATATTGTATG TACCTCTTTG CAGCCTGCTT 660 TTTTCAGTTA GTTTTTTTTG TTTTTTTGTT TTTTTTTTTT TTTTTGGAAA CCAAGTCTTG 720 CTCTATTCCC TAGGCTGGAG CACAGTGGTG CCATCTCGGC TCACTGCAAC CTCTGCCTCC 780 AAAGTTAAAC TAATTCTCCT GCCTCAGCCT CCCGACATAG CTGGGATTAC AGGCACACAC 840 CACCACACAT GGCTAATTTT TGTATTTTTT AGTAGAGACG GGGTTTCACC ATGTTGGCTG 900 GAATGGTCTT GAACTCCTGA CCTCAAGTGA TCCACCTGCC TCAGCCTCCC AAAGTGCTGG 960 GATTACAGGT GTAAGCCACC ACACCCGGCC TAGTTTGATA TTCTTAATGT GCCCAAAGTA 1020 TTCTCCTGTA ACATTTTTTA ATAGCTACAC AATATTCAAA CACACAGATA TGTTATAATT 1080 TATTTACCCA ATACCCTATT ATTGGAAAGT TGAGTTCTTT TTTTTCTTTG TTTTGTTTTG 1140 TTTTGCTACT ATTCTAAAAT GCTATAACGA ACATCCCAAT AGATACATCT TTGTATACAT 1200 CCATGGTGAC TTCCATAGGA CAGATTCCCA GCAGTAGAAT TGCTGGGTTG AATGATATGC 1260 TTAGGTAATG ACAGAAGAGT CATTTCAAGC AGCTTCCTAG GTCTAGAACT AAGGATTAAT 1320 GAGTCTCCCG CCCCCTCCCA GTCTATTCAG CATGATCTGG ATCATGAGGA CTGAGATCTG 1380 GAAGAGACTG AGATCTGGGA GAGGCTGAGA TACCAAAAGC CCTGGCTCCA CCCATACCCC 1440 TCGCCCTGAA AACAGCTCTA GGAATTCCGC GGCCTAGCAA GGCTCCGGGA AGCTCCTTTT 1500 AAAGCTGTTA CGTTAGTAGG CACATGGAAG CCATAGAGAG CCTATCCAGG GCTCATGGGA 1560 CTTTAGTGAT CCTGCCCTTC TGCCAAGGAT CCCCCATGGC TGCAACTTGG AAATTTCTGC 1620 AAATGGAAGA GCTACTCCTT AGGCACGGTC ATGTCTGAGC AGGGATCTCC TCGGGCTTTC 1680 TTAGAATTCT CTCCCTGGGC ACTGGGACTC TTGATTTCTT GAATATTATG TTCCAGGTGG 1740 GTGTGGAGGA GGTGAGGGGA TGTAAAGAAG GCTAGACTTG GCCAGGCGCA GTGGCTCATG 1800 CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCGGGTGGAT CACCTGAGGT CAGGAGTTCG 1860 AGACCAGCCT GGCTAACATG GTGAAACCCC GTTTCTACTA AAAATACAAA AAATTAGCTG 1920 AGCATGGTGG CACGTGCCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG GAGAATCGCT 1980 GGAACACGGG AGGCAGAGGT TGCAGTGAGC CGAGATCGCG CCACTGCACT CCAGCCTGGG 2040 CGACACAGCA AGACTCTGTC TCAAAAAACA AAAAAGAAAG AAAAAAAGAA AAAGCTAGAC 2100 TTACATGTGT CACTTAACCC CTTTTCTCAA CCTCTTTCTC TTCCAGGAAT AGTCAACCCT 2160 GGATGGCTTC AGGGGAAGGG GGATCCTGAA GCCCAGGGCA GCCTCCAACT CTACCCCTTC 2220 CTCCTTTGAA GGATACTAAG GGGTCCAGAA AGGAGGGGCA GGACACTGTT ACCCACCCCA 2280 CATCCCAGCA TCCACATTGC TCTCTGATGG TCAGGACAGA GCCTTCTCAG GGAGACCAGC 2340 CTGTCTGGAG CTGTGTCTCT TGGCACTCTT AAAGGGCCAC TGAAGGTCCG TTCGTGGTCG 2400 TGAGGCACAC TTTCAGGGAG CAGAGTGGTC TGTGTCTTCA CAGAGCCCGG AAAATGAACT 2460 AGTATGAACT TTGCCTCCAA GCAGCAGAAC TTCTGTTCCC CCGCCCCTAA TGGGTTCTCT 2520 GGTTACTGCT 2530
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