Tag | Content |
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EnhancerAtlas ID | HS129-00586 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:24615760-24618530 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:24616454-24616465 | AAGCAATAAAA | + | 6.32 | ZNF263 | MA0528.1 | chr1:24617148-24617169 | GGAGGAAGAGAGGAAAAAGAA | + | 6.5 | ZNF263 | MA0528.1 | chr1:24617141-24617162 | GAAGCAGGGAGGAAGAGAGGA | + | 6.74 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26668 | chr1:24615522-24618794 | Esophagus | SE_35109 | chr1:24616022-24618226 | HeLa | SE_64493 | chr1:24616030-24617222 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I024289 | chr1 | 24616197 | 24617447 |
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Enhancer Sequence | AAGGATGAGG ATTGACTGGT GATACTTTTA AGGTTCAACT TGGCATTCTG CGAGCTCCCT 60 GGTGCCACGC CAGGCCTCTG GTCAGCTGTG TGACCTTAGG TGTCCATATC TGAACTAGAT 120 TTCATCTCCT TTGCAGAGTT GTTGTGAGAA TTAAATGAAA TGATGTCTGT AAAACACCTA 180 GCACAGTGCC CGATACACAG TAGGTGCTAA AAAACCGGCC ATTATGAGAT GGCTCATGCC 240 TGTAATCCCA GTGCTTTGGG AGGCCAAGGT GGGAGGATCA CTTGAGGCTG GAAATTCAAG 300 AGCAACCTAA GCAACATAGC AATATCCCCT CTCTAGAAAA AAAAAGTTTT AAACATTAGC 360 TGGGTGTGGT GGTGTATGTC TGTAGTTCCA GCTACTTGGG AAGCTGAGGC AGGAGGATCA 420 CTTGAGCTTG GGAGCTGGAG GCTGCAGTGA ATCATGATCA TACTGGTGAC ACAGTGAGAC 480 CCTGTCTCAT AAAAACAAAA AACAAAAAAG TGCATTGTTA CTATTATCAT CATTGGCCCA 540 GGACCCTGTG TTCTATACAC AGGGTGATTT TAACCAAGGT TTAGAGAAGG CCTGTCTGCA 600 CCAGAACTCC GGGCTGGCAT CATTTTCATA AATTCTTTGT CCCATTCAGC TCCTCTCTGG 660 CTATTCAGAA AATAATCTGA ATGTTGAAAC TTGTAAGCAA TAAAAGGATT TCATGACACA 720 GGCCAAATCA GGACTTTTCC GCTTTGCAAT GACAGCCTTC CCCTCTCCTC TGCTGTGGCC 780 CTGGCTCTCC ACTCTCTCCT TGGGCTTCCC ATGGGACTGC TTAGCATGGA TCCCACGGGG 840 TTATGGTTAA CAGTCAAGAG TCCCGGGCGC AGGGCCAGGA TGGCAACTCG CCCAGGGCAG 900 GAAGCAGCTT ACGCATCAGT ATTCCCCATA CTCAGCACAG GGCCTGGCAC AGATCAGTGC 960 CCTGTGAAGG GCTATGAGTT GAAAAAATAG TGACCTAGAG TGTACTGGGT GTCTCACCCA 1020 AACTTCCCTG ACACGGAATA GAAAGCGATG AACAGAGTTA GCACTCAATA TGTATTTGTG 1080 GGCCGGGCGT GGTGGTTCAC GCTTGTAATC CCAGCACTTT GGGAGGCTGA GGCGGGTGGA 1140 TTGCTCGAGG TCGGGAGTTT AAGACCAGCA GGGCCAGCAT GATGAAACTC TACTGAAAAA 1200 AAAAACAAAA ATTAGCCAAG CGTGGTGGTA GGTGCCTATA ATCCCAGCTA CTGGGGAGGC 1260 TGAGGCATGA GAATCTCTTG AACACATGAG GTGGAGGTTG CAGTGAGCCA AGATTGTGCA 1320 CTGCACTCCA CCATGGGTGA CAGACCGAGA CTCCATGTCA AAAAAAAAAA AAGTATTTGT 1380 GGAAGCAGGG AGGAAGAGAG GAAAAAGAAG GAAAGAAGAG GCATGCCTGA CCCACCAACT 1440 GGATGACCAA ACTATGAAAG AACCGAGAAA CGAATGAAAT GGAATTCCTC TCGTAGTTCT 1500 CCTTCTCTGG AGAACTCTCC TTCTCATCAT TGGAAAAGGA GATAAATTAA ATGAGTTGGT 1560 CTTTTAAATA ATAAGCGCTA GCATAATAGC CGTATTTACC ATGTGACCAG CTGTGTTCTG 1620 TTCATTTTGA GTGTATTAAC TAATTTAATT CTCACACCAA TTCTAGGAGA TGTGTTACTG 1680 TGCCCATTTT ACAAATGAGC AGACCAAGGC TCCAAGAAGC CAAGTAACAA GCTCAAGGTC 1740 GTGTGGCTGC TTAGTGGAGC AGCTGGCTCC AGAGGCTGCC CTCTGGGCTG CGATTGCTTT 1800 GGTCCCTCTG AGGTGTTTCA GGAGGTGGAC CCCCCCACAG GTGGTGATGA CACAGGGCTG 1860 GTATTGTGCC CTGCTCATCC TGTTGCTCAG ATCCTCAGGT GTGGACTCCT TTGCTTGCCT 1920 CTTGCCCATT TCTCCACAGT CTAGCTCTAA CAGACATTTT CAGTTTGATC TCCTTCTACG 1980 TCCTTTCCCG TACCCGATGC TGCACCCAAG CCAGCTACTC CCTGTTCCCT GCTCACACCC 2040 TGTGCATTCC TGTGTCTAGG CTTTTCCTGC TGCTGTTCCT TCCTTGGCCT GGAATGTGTT 2100 CTCCCACCCC CGACTCTCAC AATCATCCCC ACCTCTCCAA GTCCAATTCA GGTGCCACTT 2160 TAGCTGTGAA GCCCTCGCTG GCCATCCCTG TTTAAAATGC ATTACGCCTT GCCCTGCTCT 2220 GGGCTTCAGT AACTAACTCT TGATCATCTC CAGCCCCCCA CATCCCACCC TAAGAAACTC 2280 TCATTGACCA GGAGCCGGGC TGAATTTCTT CACCCCTCCC CACCCCAGAT GTTGAGATTT 2340 GGGAGAGCAA GGAGCTCTGT CTAGCTCATA TCCTTGTCCC CGCTGCCCAG CATAGGACCC 2400 GGCATAAGTA CACTAACCGT AAAAGCATGG TTAAAAGTGA CCTACTCCAC TTTCAGCCAC 2460 TAGCTGATGA CGATGTGCTG GTGTCCCACA CCTTCCATTC CAGGATTCCT TCAGGTTCCC 2520 TCAATACACT TCCCACTACA CCTCTGTGCC TTGGCCATGC TGTTCCTTCC ACCTGGAATG 2580 CTCTCTCTAC CTCGGCTGCT CAGAGAATCC AGAGTCTTTT CAAGTTCAGT TCAATGTCCC 2640 TTCCTCTAGA AAGCCTTCTC CCTCCTTTGC CCCAGAGCTA AATCACTTCT TCTTTTGCGT 2700 TGTCTCCGCA CTTCACACCT GCCTGGGGGT TTGCTAAGCT GTACTGCAAT GAGTTTTCCT 2760 GTCTGTCCCA 2770
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