Tag | Content |
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EnhancerAtlas ID | HS133-03479 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:212655280-212657670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:212657046-212657056 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:212657046-212657056 | GGCACGTGCC | - | 6.02 | IRF9 | MA0653.1 | chr1:212657159-212657174 | AACGAGAGCGAAACT | + | 6.17 | KLF4 | MA0039.3 | chr1:212657543-212657554 | CCACACCCTGT | + | 6.14 | MEF2C | MA0497.1 | chr1:212656484-212656499 | GAGCTAGAAATAGAA | + | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35302 | chr1:212655268-212663203 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 212655370 | 212655477 | chr1 | 212656151 | 212656660 | chr1 | 212655326 | 212655600 | chr1 | 212655600 | 212656600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I212481 | chr1 | 212655167 | 212663350 |
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Enhancer Sequence | GGCCCACCCT TTACATATTT TACAGTGCCT CTATCACAGC CCAGGCACTG TTGCAGATGA 60 TGGGGACAAA ATGAAGTGAA GAAGGCAAAG CTGTTGCTGT CTGACAGGTC TCTCCAATTT 120 ATTGGGGCAG ACAGACCACA TGGAGAGAAG AGATCATGTG TGGTTGGAGG TGCAAGGTGC 180 AGAGAGGAAG TTGGCACCAC TTGGATCTTG GCAGAGCAGG GAAGAATGAA GTGAGGCTGT 240 AAGTGATGGG AGCCAGATGT TGACACGGAC ACTCTGGTTT CAGTGGGTCA TTGGTCAAAG 300 CTGATGTACA GGCAACCGGA AGAGACTGGT CCTCTTGGAC TTCTTCCCTT ACTATATTGT 360 TTAATCCTGT CTTGGTTAAG ATTGATTAAA TAGTAAAGCA ACTATTTTCT GTTTGGTTGA 420 CTTCAAATAT GTGGCATGGG TGAGCCATTT CCTCAGGGCA TCTTCAGGAT CTGACTGAAG 480 GATCCAGCCC AAGGCCCTGT GGGTTTGAGG GGAGGAGAGG ACACAGTCCA GGAGCCACCT 540 TTACCTGTGG ACTTGAGGCT CCTTCCAGCC CTGACCAATG ACAGGAGCAT GGCAGAGGGA 600 AACCAAGAGA TTCTGAAGGA GGAGGAATGT TCAAAGGGCA AAAAGCTCTC AATTTTATTA 660 ACTCTTGAAT AAACAACTCG TCCTTAGGGA CAGATGAGTA ACCCAGGAGG AACCCAACTC 720 TATGAAGGGC AGAGTTGCAT TCTATTGCCC TAGGAAACAA CAAGGGAAAA TGAGATTCCT 780 CTGTTATCCT GAACATGGAT TATTCTTGTC CCCCCTCCCT TTTTTTAAAT CATTAGAGGG 840 ATTTATTTCC TTTCCGGAAG AGTCACTCTT CTGCGGTCCT TCCACACCCA GCTTTGGACT 900 GGGCCACCTG GCAAGGGTGT GAAGTGGACT TGTGGTTGAT GATCTAAGGT TCTCCAGCCA 960 TACACATGTT TGGGTCCAGC CATTGGCACC AGGTGACTCA GCCTTTGAGC CTGGCCACGC 1020 TTGGTCAGGA ACACGTGAGA TCCCCAGCAT GTGACCAAGC CTCAAGCATT CATGTGGGCT 1080 GTGGACACGG AGGCTTAGAG ACAGCATAGT GGGAGCCCAG AACCACAACC AGTAGCCCAA 1140 GGATTAGTGA GCCAACTGCA AGTGTGCGGA ACACAAGAGC ATCATTTTCT CCTGCTCCTC 1200 CAGGGAGCTA GAAATAGAAC TCTGCCCTTT GTCCTTGAGG AGCTGAGGCA ACTGCCTGGC 1260 ATGGCGTGGG TGTTGGTGAC CACAGGCCCC TTTGTTCCTC TCTCCCACTC ACCCTCCCGC 1320 TCCTTCCTCG CTCCTGTGAC CCTCGGTCCC TGGCCCGTGG AGACTGTGGG CAGGGCTCAG 1380 GGCCACTGGG TGGTGTCTGG GTGAAGGTGG CTGCTTAGCA CTGGCACATG TGGAGAATGT 1440 GGTGGTGAGC TCCCTCTCAG CTGCCGTTTC CTGGCCGGCA TTAGCGTTGC CACCCAAAGC 1500 CTTCCCAAGC GTGGCTGACC CTGACCTGGG GCATTCAGAA GTGTCTGGCT TCTTCCTGGC 1560 AGTAACTTCG GTGTCAGACA CGGGCCTCTA GGGTATTGTT TTTCAAATGT CATTAACTGG 1620 CCGGGCACAG TGGCTCATGT CTGTAATCCC AGCACTTTGG GAGACTGAGG CAAATGGATC 1680 AATTGAGGTC AGGAGTTCGA GACCAGCCTG ACCAACATGG TGAAACCCCA TCTCTACTAA 1740 AAATACAAAA ATTAGCCGGG GGTGGTGGCA CGTGCCTGTG ATCCCAGCTA CTTGGGAGGC 1800 TGAAGCAGGA GAATCGCTTG AACCTGGGCG GTGGAGGTAG CAGTGCACCA AGATTGCGCC 1860 ACTGCATGCC AGCCTGCGCA ACGAGAGCGA AACTTCATCT CAACAACAAC AACAAAAAAA 1920 GTCATTAACT GAAACCCATA GTGAAAAACA CTTGTACTTT ACTTTGCATC CCGTGCACAC 1980 ATTATATACT GGATGTTTCC ACTGAACGGC CTCCTCCCTG GCTCCCCTGC TCTCAGTTTC 2040 CCTTGGGTTC AGCGGCAGGG CAGGCCTGGC AGGACTGCAG AGACAGGGAG AAGGGGGAAG 2100 TACTTACTCC CCAGTGGGGT TGCCACAGGC TAGCTGGTCC CTCACCTGAT GATCCCCGCT 2160 CTTTCCACAT CATTCTCTGT CTCCAAGTTC TGAAAACACT TTCCTCCTTC AAGCCTTCAA 2220 GCCTAAAGGT GATAAGTGAG CCCCACTGTC CCTTATGATT TACCCACACC CTGTCCCATC 2280 TTTGTAAACA GCCTCTATCA AATGCTCCGA GAAATTATTC AATTAGAATG TGCTGTTTTT 2340 CTATTTCAGG GGCATTGGCT CAAGTTTATC CATGTATTAT GTGTGTGTAC 2390
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