Tag | Content |
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EnhancerAtlas ID | HS129-06199 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr11:18267600-18269460 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr11:18267941-18267958 | CATGTCATTGTGACCTG | - | 6.64 | ESR2 | MA0258.2 | chr11:18267942-18267957 | ATGTCATTGTGACCT | - | 6.27 | IRF1 | MA0050.2 | chr11:18268389-18268410 | AGAGAGAAACTGAAAGTCCCA | - | 6.65 | IRF1 | MA0050.2 | chr11:18268068-18268089 | TTGCACTTTCTTTTTCTTTTT | + | 7.23 | ZNF263 | MA0528.1 | chr11:18268868-18268889 | GAAGGAGGAAGGAGAAAGAAG | + | 6.98 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I018245 | chr11 | 18267173 | 18268958 |
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Enhancer Sequence | AAGGAAAGGA AAGGCAGAAG GGACATCAGG AGAACATAAA GACTCCAACA ACACCTTAGA 60 GGGGAATGAA AGAAGGACAA ATCTTCCACT GACTTCAAGC TTTCAGCCTG TGATCATAGC 120 AGCCTTGGAT ACCATGGGTT GAGAAGCACA TTCCTTTATC CTAGTTGGCT TCTTCAAGTG 180 CCCTGGTGAA GAGCCACTGC TATAGAATGA AGCTGCCTAT GATAAGATCC AGGAGTGTAT 240 ATGAATGAGG TGGTGACATG GAATACTGAT GCTGAGAAAG GTGGCAGACA CAGAGTACTT 300 CTGCCCTGAC TACTAAAGTA TATATTCTTG CAAATGGAAT ACATGTCATT GTGACCTGAG 360 TTCCAGTGAC TGTTAGGAGC ATAAAAGTCC CTAAACACTT TCTCAGTAGG CTGTACTGAT 420 ACTGTGGGTT GCTTGAGGAA GCAATAGAGC AGCGGTTCTC CGCCGTGGTT GCACTTTCTT 480 TTTCTTTTTT ATTTTTTTAG ACGGAGTCTC ACTCTGTCAC CCAGGCTGGA GCACACTGGA 540 GCAATGTAAC TCACTACAAC TTCCGCTTCC CGGGTTCAAG TGATTTTCCT GCTTCAGCCT 600 CCTGAGTAGC TGGGATTACA GGTGCCTGCC ACCACGCCTG GCTACATTTT CATATTTTTA 660 GTAGACACAG GGTTTCACCA TGTTGGCCAG GCTGCTCCGG AACTCATGAC CTCAAGTGAT 720 TCATCCACCT TGGCCTCCCA AAGTGCTGGA ATTACAGGCG TGAGCCTTGG CTGCACTTTC 780 TAATCACCCA GAGAGAAACT GAAAGTCCCA GTGCCCAGGC CACACCCCAG GCCAGTTTCT 840 GCAGACTCTG CTGGGGAGTT GAAGGCATGG GTAGTTCAGG TGATGCCAAG GTGTGTCTGA 900 GATTCATAAC CATCAACCTC TGGGAGGTGG TCAGTGATGC GTCTACCTGG CAAGAGCCCT 960 GACCTCAAGC ACAGCCGGGC TCAAACCTCT GCCCTGCCAC CTGCTGACTG GCAGTAAGTC 1020 CCTGGGCATT GGCCTCAGCT GCTCTAAGTC TCAGCTTTCT CACCTTCACA GAAGGGATGC 1080 CTGCCTCACA GAGTCATTCT GAAACTAGAT GAGAAAATGC TGTGGTCCTT GTGGGGGCTT 1140 GAGGCACGTT AGTTCCCAGC TCTTGTCAAG AAGGCTGGAG AAGGAAGAAT GGAAACAGAA 1200 CAAACCAGGA AGGGAGCCCC TGACAGAGCG AGGCTAAAGA GCCCTGTACA TTATCCAACT 1260 AGGAAATCGA AGGAGGAAGG AGAAAGAAGA CAGAAGAGTC AACAGCCTTA GTCATACTCC 1320 TATGCGATTT ATGCTGAGGG ACATTTTATA CCAATTGCAG GCCTTATTTT GCATCTTCTA 1380 CTCAAAACAA ACAGCTCAGG TGCTCCTGGA AAGGATGATT GTTCTTTCTC TGAGTAACTG 1440 ACAACAATCC TCGACTCTCT AATCTGTTTA GCAGCTCCCC AGGCACATTG GGCAGCACAA 1500 CCTAAGGCAG CGGCTCAAAT CTTAAGGAAG CCCAAAAATA CCCCGTGTGC GTTGTTACTG 1560 GATGCCCCGT CCCTTACGGC TCAGGAGATG TGTTTTTGAT ACACCTTGCA GCGGCTTCTG 1620 AAATGTGATC CATCCACTTA ACACATCCTG AGAAGCTGCA CTACGGGGAA AGGGGATATT 1680 CCCAGCAGCT CTGAAAGACT CGAGACAGGC AACCCAGCAA ACCCTAGTTC CTGGCAGGCC 1740 TCAGCAACGC AGACACTAGC AACTCTGTGG TTCAAAAGCA GCCTTCCGAA AGCATCATTT 1800 TCCCCAGTTT ATCAGGTCCA GGGCGATGTT TCTCTTCAGA AATCCTGCAA ACCTTCTGAA 1860
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