| Tag | Content |
|---|
EnhancerAtlas ID | HS133-30437 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr8:38482790-38484710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:38483174-38483192 | TGAAGGAAGGAGGGAAAA | + | 6.17 | | EWSR1-FLI1 | MA0149.1 | chr8:38483170-38483188 | AGAATGAAGGAAGGAGGG | + | 6.63 | | RARA(var.2) | MA0730.1 | chr8:38482919-38482936 | TGACATTCTGATGACCT | - | 6.01 | | ZNF263 | MA0528.1 | chr8:38483175-38483196 | GAAGGAAGGAGGGAAAAGGAA | + | 6.12 | | ZNF263 | MA0528.1 | chr8:38483026-38483047 | GGGGCAGGAGGAGAAGAAGGG | + | 7.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I038625 | chr8 | 38482808 | 38484665 |
|
Enhancer Sequence | TGTGGACCAG AATGGCCTTT CTTTATTAGA AATGAGCAGG GTTGGACGTG GACCCATTGG 60
TGAGTATGGA CCATGCCAAG TGGTGGGTGT TTGCTACTGA TTTCAGATAT ACTCCTGCCC 120
TCAACAGGTT GACATTCTGA TGACCTTCTG TCTTCTCTAT GTATTTAAGA TGCGTAGATG 180
TCCCCAAGGA CGTGAGAATG CCAGCATTCT ACCTCATTTA ACCAGAGGAG ACTCACGGGG 240
CAGGAGGAGA AGAAGGGCAA TGGAGAGAGA CAGACACCTT GCAGAGAAGT GGGTGGGAAG 300
GAAAATGGAT TCAGGCACTT TCGAGTGTCA GAGAAGTGGG GCTGGGGTGG AATTTGAGAT 360
GGGCAGGGAA TTGGGGGTGA AGAATGAAGG AAGGAGGGAA AAGGAAGCAA GAGAGTGTTT 420
TTATTTATTT ACATTTTAAA TGGAAACAAG TGCATGGAGA AAAAGAGAAG GAAAGAAGGG 480
AAAGAGATGA GGGCAATGTC ACACAGAGAA TCTTCAGACA CTTTAAAATG GACCTTTACT 540
TCCCTGCAGC AAGGAATCAA GACAGCTTTT TTGCGAACAT GTTTTCTCGT GCAGCTGTGC 600
AGGGTAGATG CCACATGTCA CTTCCAGATC CTGGTTCTTC TGAGAATATT TTTTGAGGCT 660
TTTTCTTGCC TTCCTAAGGC TGCCTGGCTA GCCAGCTAAT GGTAAAGGCT CTCACTTCTT 720
CTCCCCTCCC CACCACCCCA TCCCCAGCTC CCTCTCCCTT TCCTCCGCCC CACTGAACTC 780
CCTCTCCTCC TCTCCTGGGC AAGCCCAGGC TCCTCCTGCA GGAAAGGGCA GCCAGGATTG 840
TGCCAAGCAG CCCACAGCTC TGGCAGAAAG TGCTGGAGAA ACTTTAATGA ATTCAAGACC 900
TGCTGGGCTG TCCCAGAGAA AGAACTGGGC TTCAGCCTTG CAGGAAGAAG CAGAAAACTG 960
CCCCCTTGTC AGGAAGATTT ACGCCCTGGA GGCCCAGCAG GCCCTATTGC ATCAGGCAAG 1020
CAATTACTTG GAAAACTACA TTTTGTTGAA ACAAAGAACA CACAAAAAAC CATCGAATTC 1080
CTTGCTGCTA CCTCCCCCAC TGCCACTGTA CTTCCCCAAG TCGCAAAGAA CTGGGATTTG 1140
GCTGCTTTGA AATCAAATGA GTGAGCTGCA AGGCTGGACC CAGAGGAGAA GCTGCCCTCT 1200
CTAGGGAGAT GAATGTGGAG GCAGTGAACT GCCTCCAGCC CAGGAATTAC CTCTTGTTGG 1260
AACCGTTTAC CCTTCTAGTG CAAGCATCTT GGAATTCCCT CATGCTGGGG TGGGGCACTG 1320
TGGGCTTCCA ACTCCAGAGG CAGTTTCCAG CCCTGCAGCC CTGCTACAAG ATTAGCGGCA 1380
ACTAGGCTCT GCCTAGCTCC GAAATCCAAC TGGTTAGGAG CAGCCACAAA ATGTAGGTCC 1440
CCAAAGGCGG CCACAAGTCT CTAGAGAGTT TTCTGTGGGA CTTGATTACT GTTTTCAAAT 1500
ACTTAAAAGG CTGTCATTTG GTGAGGGATA GATTTATTCA GTGTGGAGCC AGAGGATAAA 1560
ATTAAGACCA AAGGTGGACG CTGTAAGAAA GCAGATTCAG GGCTCAAGAA AAAGAACAGT 1620
TTTGCTGCTA ATGTTATCGG GCAGGGTAAT GTACGGCCTT GGTAGGTAGT GAGTTCCCCA 1680
GCACTGGAGG TGTTCAAATA GAATTTGGAG AAAGTCTTTT CAGTGTTTGC TGTCTCCCAC 1740
ATGTACTTCT AGGGGATAGG TACTCAGCTT TTCATGTCTG TATGCCGTGC CTGGCACAAA 1800
CATAGCAAGG ACTGGATGGC TGTTGAATGA ATTAATGATT CAGTGGGTTA CATTAAATGA 1860
CATTTAAGAT CTGTTTCAAC AATGATGTGC TGGGGGTTCT GAGTGTTTTC TCACTCTTCA 1920
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