Tag | Content |
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EnhancerAtlas ID | HS133-29614 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:127740340-127741750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr7:127741491-127741502 | ATGACCTTGAC | - | 6.32 | Esrrg | MA0643.1 | chr7:127741491-127741501 | ATGACCTTGA | - | 6.02 | Nr5a2 | MA0505.1 | chr7:127741490-127741505 | CATGACCTTGACCCC | - | 6.05 | RREB1 | MA0073.1 | chr7:127740852-127740872 | TGGTAGGGGTTGGGGTGTGT | - | 6.43 | ZNF263 | MA0528.1 | chr7:127740486-127740507 | GGAGGTGGGGGGTGGGGAGGC | + | 6.17 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_60951 | chr7:127740843-127758458 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TTGTAAAGCA CTTTACACAG GGCCCAGCAC AGATTCTGTG TTCAGTGTTT GCTGTTATCA 60 CCCAGGGAGG AGGGTGCAGG CATGGAATAA CCTCTCTGCT CTTGAGAGCA TTGTGGGGTT 120 GAGGCCAGAA GGGAGTCAAG GTGTCAGGAG GTGGGGGGTG GGGAGGCTGA GATGACTGGG 180 CTGAGTCTCT GGCTGTCCAG TTGTGGAGTG ATGGGAAGCA GGAGTCATGC ACACCCAGGG 240 CAGGGGGTTC CATCCCTTCA CCTTGCTGGC GTGGAACTAG TCCTGTAGCT AAGGTGTTCA 300 GCGCATGTGC ACTGAGTACC TGTCGTGCCA GGCACCATTT GGGTGCTGAA GTTACAGAAG 360 CAAACAGCAC AGAGCTCCTG GCTGCATGGA CTAGGGAGAG GACATATGCC CATACTCACC 420 TGGCATGGAG GACACCATGC CTAGCCAAAA CTTACACATA GACACTTTGC CTCAGACCTG 480 AAATCTGGAT TTAGACAGCA GAAGGAAGTT AGTGGTAGGG GTTGGGGTGT GTGTGTGTGT 540 TTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTAGATGCCT CTTGGAGGAG CCAGTTCTGA 600 TTCACAGACC TGAAAACCAG CAGCAGAAAA TGACTCCTCC CTGCTGATGT GGGTGTAGTT 660 CTGGAGAAAG TCCTGTGCTG GGGCTGAGTG GACCATGGGC AGGGAGTGGG GTGGAGCAGG 720 GGCAGTGCTA GGGGGCAGGA TGCTGCAGTG CACCCCACCC ACCATGGGAA GCCCCGAGAT 780 GGAGTTTACT GGGGCCTGGA TGCAGGGGGA GCAGCCAGTA TCACAGCTGC ACTCCTGCCT 840 CGACTCCAGC ACATAGGCCT CACTGGCTGT GAACAGGGAA ACACTAGTCT CAGGTTCCCA 900 GGGAGCAGAG CTATGCAGAG GGAGCCCTCC AGAGTCAGGC GAAGGGCATC ATGCCAGGCA 960 GGAAGTATTA GCACTGATGT GGGGGCACCT CCTAGGCCGT CCTCATGTCC ACTGTGTGAG 1020 TGGCACACAG TGCATGACAG TTGGGGACAT TCCCATTTGA CAGGGTGACA AACCAGAAGA 1080 GGTGGGTGCC TGATTCCAAG TTACACAGGG TGTGAGGAGC TGCACAGAGG CCACCATGAT 1140 GAGCCACTTA CATGACCTTG ACCCCTAGTG AGAAGGACCC GTGTGGGCAA AGACAGATCT 1200 GAAGCTGCAC TTTACTCAAC AGCTGGGGAG GGCCGTTTCC AGAGGGGGCT TCACAAGGTG 1260 CAGTCGCACA GGCACTCGGG TTTGCAGGGA GGAGGATGTC CTTGGGAACT AGCCTGGCGG 1320 CCTTGTCTCA TCTGGCCTGA TCTGTAGAGG GCAGCTCCCA GGGGGGAGAC CCGAGGCAGA 1380 GATCACAAAT AGTGCCATGT CTGATCAATT 1410
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