Tag | Content |
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EnhancerAtlas ID | HS105-20600 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:115099880-115101180 |
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) |
CTCF | MA0139.1 | chr12:115100576-115100595 | GCACCAGCAGATGGCGGCA | + | 6.4 | STAT1 | MA0137.3 | chr12:115100411-115100422 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr12:115100411-115100425 | TTTCCAGGAAATGG | + | 8.42 | ZNF263 | MA0528.1 | chr12:115100690-115100711 | TTTCCCCCATCCTCCACCTTC | - | 6.08 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I114662 | chr12 | 115099697 | 115101283 |
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Enhancer Sequence | ATATGGCAAA ACCCTGTCTC TACCAGAAAT ACAAAAAAAA AAAAAAATAG CCAAGCAAGG 60 TGGCACAAGC CTATAGTCCC AGCTACTTGG GAGGCTGAGG TAGGAGAATT GCTTGAGCCC 120 AGGGGGTAGA AGTTGCAGTG AGCTGAGATT GTATGCCTCT GCACTCCAGC CTGGGTGACA 180 GAGCCAGACC CTGCCTAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA 240 AAAAAACCTC TGTCTTTGTT GGAATTTCCA AAACGGGAAG GAAGTAGGAA CTATTGACAG 300 AGCAGGTGCT TTGCAAGGAT ATTTGTCCCT TGCTCTTTAC AGCACATCTG CCTGTAAGGA 360 TGTGGGTATC ATTATTCCAC TTTTATTTTA TGAGGAATTA AGACCCAGAA AAGTTAAGCC 420 ACCTGGCCAA AGGACACTCA AAAAGTAGGT GGCAAAGCCA GGACTCCAGT CCCATTTTTC 480 TGCCTCCAAA TTCTAGTTAT TTGCCTTGCC ACCATTCTCT CTATCTCTTA GTTTCCAGGA 540 AATGGCCATG GGGTTTGCTT CACTGGAATG CAATTCCATG AGAACAGAGA CCATGTCCCA 600 GTGATGATTA ATTGCTGAAT AAATGAATGA TAACGTAAAT GAGTATGTGA CTCAGCCTTC 660 CAGAAGTATT GGAAAAGCCC CATGCACTTT CCTATGGCAC CAGCAGATGG CGGCAAAAGA 720 GCAGCTTAGC AAAGGCAGAG GCAAACACTT GGCGTTTCTT TCATTTATGT ATCCTCTCTT 780 CCTTGATCTT TGCAAAACAG GTAGCTTGCA TTTCCCCCAT CCTCCACCTT CACTACTCCC 840 CTCCCCCCAT TCTGGGAGGA ACCAAGAGGT AGTGCTCACA GACTGCAGTC CCCTCTTTCT 900 GTTTTGACCT CTTTGCCCCA CCTCAGAGAC AAGGTTATTT CAAGAAATGG AAGAAGAAAT 960 AACACCAGAA GAACTTTAAT GGCAATGAAA ACCAGTGCAG AAATGACCTT TTTATTGACA 1020 AATAGAGAAA AGGTATCATG TCCCCAGCTG CTGATGAGGC AGACACAGAC TGTCCCCCAA 1080 CATTGGCCTC ATCATCCATA CTTTTGTGAT TTGCCTTGAA GGGAAGTATG GGGTAGAATA 1140 GAGGTGGGCA GGGGGAATTT CTTGTTGCGA GGAACTGAAA CGGAAGTGTT GGGGATGGGA 1200 TGGTGGCAGT GGAGAGGAGA GGGTAGCCTT GGTTTACATC ATTTTGTTTG AAATCAGTCT 1260 TGATTTCCTT GACGCCAGGA GGAAATCCAT CCCTAAGTGG 1300
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