Tag | Content |
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EnhancerAtlas ID | HS108-10766 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:122369790-122372150 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:122371315-122371333 | AGAAGGAAGGAGGGAAGA | + | 6.77 | Foxq1 | MA0040.1 | chr12:122369947-122369958 | TATTGTTTATT | + | 6.62 | RORA(var.2) | MA0072.1 | chr12:122370305-122370319 | GTTAAGTAGGTCAG | + | 6.34 | SCRT1 | MA0743.1 | chr12:122371239-122371254 | GAGCAACAAGTGTTC | + | 6.12 | ZNF263 | MA0528.1 | chr12:122371313-122371334 | AGAGAAGGAAGGAGGGAAGAG | + | 6.02 | ZNF263 | MA0528.1 | chr12:122370323-122370344 | CCTTTTATCCCTCCCTCCTCT | - | 6.2 | ZNF263 | MA0528.1 | chr12:122371316-122371337 | GAAGGAAGGAGGGAAGAGGGG | + | 6.95 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121933 | chr12 | 122371041 | 122372401 |
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Enhancer Sequence | AGGTATGCAG GGATTTCCTT CCTACAGGTG GGGGAGTTGT CTTTAACGTG CGTGTGGTAT 60 TTTGTTTTGT ATCTCAAGGG CTGACTTCAT TCTATCACTG TCGTATTTTC CCACTCTCCT 120 TGGAACTAAA AGCAAGCCTG TCTTTAGAAA CACATGGTAT TGTTTATTGT CTCTCTGTTT 180 CTAATCAGAA TCAACTTACA AAACAGCAGT TGATATTAAT TTTATAGTGA GAATTTAAAA 240 CATCTGTATT TTTTACACTT CTGCAAAAAT GTGGACAGCG TAGATCATAT CTCCACAGAT 300 ATAACACAAA GGGCAGCTAT TCAGCAGGGT GCCGACCTCA CGGACACTTA CACACATCTC 360 TAGTTTTCAA AGGGCTTTCA TCTTATAACT GTACCGAGAA GTGGGTATTC ATATATCCAT 420 TTTACAGAAG AAGAAACTGA GGCTCAGAGT GTTTTAAGTG ACTTGCCCAA GACTGTACTA 480 GTAAACAATG ACTCTACATC TCCTGTCTTG AAAGTGTTAA GTAGGTCAGT TGTCCTTTTA 540 TCCCTCCCTC CTCTCAGCAG CTTTGCTCAT TTTCACCCCT CTCTGAGCCT CCCCCATTTG 600 TCCTTCATGC CTGCCCTCCT CACAGCACTC TGCCTCCTTT GTTCCTGATA TTTGGGACCC 660 ACTTCATTTT CATCATTTAC CTTTCCAAGC ATCCTATTCC TTGGTGTCTG ACTTTCCACT 720 CGTTGGCCTG GTCAACTGTT CCACATCACC CTTTCAGTTG ACGTGTGTTG TTACAGGAGT 780 GTCCTTAGCT GATGCCTAGA TCAAAAACAC CACGAGGTAT TTACCAAGGA CCCAGTCAGT 840 ACTCAGTGTT GTGCCAGGGA CTCAAGATGT CTGGGTGCAA CTTAAGGAAT TCACTCTCTA 900 GAAGTCCAGA AATACGCAGG CAGAAATCAG CAGGCAGCTC CCCTTGGAGC TTCATTGAAT 960 GCATGGCACT GAACACAGTG GTGATGGCAG AGAGAGAAGG AGAGATTGCT GTGGGCAGGC 1020 TCAGATAGTC AGGGGAAGCA GGATGCGCAG ATGGGCTGGG GTGGAAGGAG GCAGGAGTCC 1080 AGCCTCACTA GGGCCAGAGG GCTGGGAGTG GCCTTGACCA TCCATTCGTT TCACAAATAG 1140 TTATAGCTGC TATGTTTCAC AGTATAGGTC TGTAGTAATG AACAAAACAG ATGTATTCCC 1200 TGCTCTCATG GAGCTTACAG TCTAGAACAG AGACAGATGT TAAACAAGTG AACACATAAA 1260 TGATTACAAA TTGTAACCAG TGCTTGAAAG GAGATGTGAA AACGCTCTAA GGGAGAAAAA 1320 TCAGGGTAAG AGAAGACTTA ACTTTAGATT GAGTGGGCAG GGATTGAAGA GGTGCTGTTT 1380 CTGCTGAGAC CTGGAGGATG CGAATGAGCC AGCCAAAGAC AGTCTGGGGG AGAACATTCC 1440 AAACAGAGGG AGCAACAAGT GTTCAGGCCT GTGTGTGGGG CCTGGAAAGA AGGCTGGTGT 1500 GGCTGCTGCA CCATGAGGGA GACAGAGAAG GAAGGAGGGA AGAGGGGCCA TTTCCCAGCA 1560 GGGAGTGCTG CCATTTGTGT TCCCAGAAGA TTCCTCTCTT GTGTGCATAA AAGGATTGTA 1620 AGAAGATAAG AGTGGAAGCA GAGGCCGAGC ATGGTGGCTC ATGCCTGTAA TTTCAGCACA 1680 GGCTGTGGCC AAGGAGGCTG AGGTGGGTAT ATCGCTTGAG CCCAGGAGTT TGAGGCCAGC 1740 CTGGGCAACA TGGCAAGACC CTTGTCTCTA CAAAAAATGT AAAAATTAGC TGGGCACGGT 1800 GGCATGTGCC TGTAGTCCCA GCTACTTGGG AGGCCGAGGT GGGAGAATTG CTTGAGCCCA 1860 GGAGATCGAG GCTGCAGTGA GCCAAGATTG TGTTGATGCA CTCTAGTCTG GGTGACAGAG 1920 TGAGACCCTG CCTCAAACAA ACAAAAAGAG TGGGAGTAGA GAGACCAGTG AGGAACTTTT 1980 TGCCCCAGAG CTGCTCAGAG CCCTGAAGTG AGCAGTGTTC TAGAGAGAAG AGGCCGGCAG 2040 CGTGACTCAG AGTGGCTGGG GGAGGGGAGG ACCCAGATGC TTATCCTCCA CTTGGGTTGG 2100 GAGTTGCCGC TTGCCTTCAC CTCTAGGAGC CACTGTTCAT GTAGGGAACT TATCTTTCAG 2160 GTGTTTGGAG GGAGAGGAAG TTTGAAAATC ACCCACTAGG AAGTGGAGAA ACACCCAGGA 2220 AGGCCAGCGG GAACAGAATT TCCAGCCAGA TGAGCGTTGA AAGGAGCTCA GATCTTTCTG 2280 TGGGTCCCCG GCCTTTGCTG ATAGTGGCCA AGGCTGGGCC GCATCTTGGA TGTTTCAAAG 2340 CGTTTTCTCT CCATTTCCAT 2360
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