Tag | Content |
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EnhancerAtlas ID | HS101-34030 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr4:187740520-187743230 |
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) |
NEUROD2 | MA0668.1 | chr4:187740957-187740967 | GCCATATGGT | + | 6.02 | SPIC | MA0687.1 | chr4:187740694-187740708 | AGAAACAGGAAGTA | + | 6.81 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34332 | chr4:187740261-187746543 | HCT-116 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I186820 | chr4 | 187741488 | 187742362 |
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Enhancer Sequence | GGAATTTATG CTTCTCTGTC TTCAAGTTCA TGAATATTTT CTTCTGCAAT GCCTAGTCTT 60 TTTAAAATTC TATTTAGTGA ATTTTTAAAA AATCCTTCCC TTATTGGGGC AACACCCTTC 120 TGAGAGTAAG CTACCCAATG CCTCGGGTTT ATAATGTTTT CTGATATGGC TCATAGAAAC 180 AGGAAGTATT TCTGCTTCTG TGACAGGGCT TGGCACTGTT TCCTCTAGCC TTCTAATGTT 240 TATTCCTCTG GTCTTGGGTA GTTTGATCAT TGAGTATTAT TCTGCTGAAT TCTCCAGCGA 300 TGGGCTTTAC GGATTTCAGT AATTCTCTCT GGGCAGCACT TGGGCATCCT GTGAAGGATT 360 CACCTTGTGG ATGATACACA CTTTATAAAC CACCTTTTCT GTGAAGGGCC AGATGGCAGA 420 TATTTTAAGC TGTGCAGGCC ATATGGTCTC TGTTGGAACT ATTCAACTCT GCCATTATAG 480 CCTGAAAGCA CTTGCACTAT GTACATGAAT GGACATGGCT ATGTTCCAAT AAAACTTTAT 540 ACAGTAAAAC AGGTGGTATG CAAGATTTGG CCTGTGGGCC TTAGTCCATT GATGACTGTG 600 ACTATAACTG TGCCTGTGTA TTTGTGTCTG TGGGTGGCTG GGTGGGTGTA CATGTTTTGT 660 ATTAATAGTT CCTATGTCCT AAATGGGATG TGAGACAGCC TTATTCCAAA TTCAAAGCAG 720 AAAAAAGAGC CTATAGTTAT TGAAACTTTT CAGATTGGCG TACACTGACA CTTGCTTTCA 780 TTATTTTTGC TCCTGTTTTT GAAATGCTAA GTAGTGAATC GTTTAATGCT GACATTTAAG 840 CTAATTGCTC TTTAATGTAC ATTTGACATA TGAAGCAACA TATTGCAATC TAAAAATAAT 900 TAAGATAAAT CATTTGCTTA TATTGCTGTG GCAAAGTCAA ACCATTTTTC ATCTCTCTCC 960 CTCTTTCCTA GTGTTTAAAG CAGGGTGTCT TGAAGTCAAA ATGGAAATTG GTACTTGCCG 1020 CCCCCGCTTT GTGGGGGCCA TGGATGGAGG GGCTGCAGCA GCTCATGGGA TGCTCTCTCT 1080 GTCATCAGGC AGCCTCCCGA TGGGCTGCCT TCCAGGCTCT GTGCTTCTGA ATTCCTCTGC 1140 AGCGGTTGGC AGGCAGCCAG TGTGCCATGA AGGATTAGAT TCTGTCTCTC TTCCTTTTAT 1200 ACACACCCCA AGAGGATTTC CTTCTTCAAC TTTTAAAAGA CTGGCTCCAA CCAGCAAATC 1260 CAACAAGTGG GCCCATTTGT GAATTGAGTA TCTTGGGAAT TATGCTATAC AAATAGGTCA 1320 CAGTTGAATA ACCAGTATGT GCAAATTGAT TTTTCTCTTT GGGTGGGGGA AAAACCCTCC 1380 TAGTTCTCTC TAGGGAAGAT TGTATCACCA TATAACAACT GTCACAAGGG CACAAAAATG 1440 CATTTTTGAG TATGAATGAG TCATCTGTTT CTCTGGGTGC TTCATTTTTA GTTATAAAGT 1500 GCGTTGATCA TATTTCAAAA GCCTGCTGTA TGTTCTTTAA AGTTAGACCC TTTTCTCCAT 1560 TTGTGCTGAG CAAGTAAAGA TTTCCAGCTT TATTCAGTGT GATTATATAT TATGAAACCA 1620 AAAGGCTATC AGTTATTCCT ATACAAAGGC AGTTTGTTCA TTTTTGGTAA ATACAGATTT 1680 GGGCATGTGC CATTTTCCTA TATTGTAATT TTTCATGAAA AGAAGTAAAA TTTATGAACA 1740 GATTTGTCAC ATTGAGTTGA ATTTACTTAA CACATGTATA AAATGTTATG TGGAAAAAAA 1800 AACACACTAA AACTCAAAGC GCTTTTTCTA TCCTGTTATT CAACAACAAT CATCAACACA 1860 GAAGACTTAT GAGACTAAAT GTGTGAGAGT GTCTCCCACA CACGAAAGGG TATCTCCCCA 1920 CACACGAAAG GGTGTCTCCC CACACACGAA AGTGTTTCTC CCACACACGA AAGGGTGTCT 1980 CCCCACACAC GAAAGGGTAT CTGCCCACAC ACGAAAGGGT GTCTCCCACA CACGAAAGGG 2040 TGTCTCCCAC ACACGAAAGG GTTTCTCCCA CACACGAAAG GGTGTCTCCC CACACACGAA 2100 AGGGTGTCTC CCACACACGA AAGGGTGTCT CCCCACACAC GAGAGGGTGT CTCCCCACAC 2160 ACGAAAGGGT GTCTCCCCAC ACACGAGAGG GTGTCTCCCC ACACACGAAA GGGTGTCTCC 2220 CACACACGAA AGGGTTTCTC CCACACACGA AAGGGTGTCT CCCCACACAC GAAAGGGTTT 2280 CTCCCACACA CGAAAGGGTA TCTCCCCACA CACGAAAGTG TTTCTCCCAC ACACGAAAGG 2340 GTGTCTCCCC ACACACGAAA GGGTTTCTCC CACACACGAA AGGGTTTCTC CCCACACATG 2400 AAGTGGCAGA CATCTGCTAA GTGTCCCCTG ATTCAACTCA GTTCCAATGC TGTCCACCTG 2460 GAGACAGCCT CAGACCCCAT AAAGTGAAGG ATCCGTGCCA CAAGACCGCC CCTGACTTCA 2520 GACGCCAATC AGTAAGTGCA AGTGGTTTTC CTTGTACTTC TGAGCCCCCC AGCCCCCCAC 2580 CCTGGCTATA AATCAGAATT CCCACGACCC CATCCTGTGG TGCAATTAAT TTGCTAGGGC 2640 TGCTCACAGA ACGCAGGGAA ATACGTTTAC TGGTTACTAT AAAGGATATT ACAAAGAATA 2700 CAGATGAAAA 2710
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