Tag | Content |
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EnhancerAtlas ID | HS003-11847 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:115099720-115101670 |
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 | IRF1 | MA0050.2 | chr12:115101362-115101383 | GAAGAAAAAGTGAAAGAGACA | - | 7.2 | RREB1 | MA0073.1 | chr12:115101627-115101647 | CCCCAAACTACCCCCTTCCA | + | 6.82 | 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 | GGAAATTGGC ATAGGAGATG AAGAAATTTT CTAGAACGCT CAAGAGGGAA AAAATGCTAA 60 GTAAGGCTGG ACATGGTGGC TCACGCTTGT AATCCCAGGA CTTTAGGAGG CTGAGGCGGG 120 TGGATTGCTT GAGCTGAGGA GTTTAAGACA AGCCTGGGCA ATATGGCAAA ACCCTGTCTC 180 TACCAGAAAT ACAAAAAAAA AAAAAAATAG CCAAGCAAGG TGGCACAAGC CTATAGTCCC 240 AGCTACTTGG GAGGCTGAGG TAGGAGAATT GCTTGAGCCC AGGGGGTAGA AGTTGCAGTG 300 AGCTGAGATT GTATGCCTCT GCACTCCAGC CTGGGTGACA GAGCCAGACC CTGCCTAAAA 360 AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAACCTC TGTCTTTGTT 420 GGAATTTCCA AAACGGGAAG GAAGTAGGAA CTATTGACAG AGCAGGTGCT TTGCAAGGAT 480 ATTTGTCCCT TGCTCTTTAC AGCACATCTG CCTGTAAGGA TGTGGGTATC ATTATTCCAC 540 TTTTATTTTA TGAGGAATTA AGACCCAGAA AAGTTAAGCC ACCTGGCCAA AGGACACTCA 600 AAAAGTAGGT GGCAAAGCCA GGACTCCAGT CCCATTTTTC TGCCTCCAAA TTCTAGTTAT 660 TTGCCTTGCC ACCATTCTCT CTATCTCTTA GTTTCCAGGA AATGGCCATG GGGTTTGCTT 720 CACTGGAATG CAATTCCATG AGAACAGAGA CCATGTCCCA GTGATGATTA ATTGCTGAAT 780 AAATGAATGA TAACGTAAAT GAGTATGTGA CTCAGCCTTC CAGAAGTATT GGAAAAGCCC 840 CATGCACTTT CCTATGGCAC CAGCAGATGG CGGCAAAAGA GCAGCTTAGC AAAGGCAGAG 900 GCAAACACTT GGCGTTTCTT TCATTTATGT ATCCTCTCTT CCTTGATCTT TGCAAAACAG 960 GTAGCTTGCA TTTCCCCCAT CCTCCACCTT CACTACTCCC CTCCCCCCAT TCTGGGAGGA 1020 ACCAAGAGGT AGTGCTCACA GACTGCAGTC CCCTCTTTCT GTTTTGACCT CTTTGCCCCA 1080 CCTCAGAGAC AAGGTTATTT CAAGAAATGG AAGAAGAAAT AACACCAGAA GAACTTTAAT 1140 GGCAATGAAA ACCAGTGCAG AAATGACCTT TTTATTGACA AATAGAGAAA AGGTATCATG 1200 TCCCCAGCTG CTGATGAGGC AGACACAGAC TGTCCCCCAA CATTGGCCTC ATCATCCATA 1260 CTTTTGTGAT TTGCCTTGAA GGGAAGTATG GGGTAGAATA GAGGTGGGCA GGGGGAATTT 1320 CTTGTTGCGA GGAACTGAAA CGGAAGTGTT GGGGATGGGA TGGTGGCAGT GGAGAGGAGA 1380 GGGTAGCCTT GGTTTACATC ATTTTGTTTG AAATCAGTCT TGATTTCCTT GACGCCAGGA 1440 GGAAATCCAT CCCTAAGTGG CCAAGCACCA CCCAGAGGCA TTTATTTAGT CAGGGCCTAA 1500 GAGTGACAAG GGACTTCCCT GTGATCCTAT TTTAACAGAG GGGAGGAAAG AGGAATAACT 1560 ATCTTTTCCC TTGAACATTC TGCAGTGTCT AGACTATTCC TTTATGTCTG TGAATTTTCA 1620 TGTGTGGTTG GTATGTTTAC CTGAAGAAAA AGTGAAAGAG ACACAAGAAG GGCACAATGA 1680 TAGAGAGAAA ATACATCCAC TGCAACCACT ACAACCTCTG CCTTCCAAAT TAGTGGGATC 1740 CCTGGGCACA TTTAAACTTG ACCCACACAC ATGTTTTGGG TAGATGCCTA CTTTGTTCTA 1800 GGCTTTGCTG AGCAATGAAG AGAAAGGGAA TTACCTGCAT TGAAAGAGGT CCAAGCCTCC 1860 CCCTTGTTCA TTTTTGCCCC AAGGAAAAGA TTCAGGTGAT TCTCAGGCCC CAAACTACCC 1920 CCTTCCAAAC TATTCACTCT GATGTTCCAA 1950
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