| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08307 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr12:133484500-133486020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr12:133484539-133484553 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGGCCAGTC TGGTCTCGAA CTCCTGACCT CGTGATTCGC CCGCCTCGGC CTCCCAAAGT 60
GTTGGGATTA CAGGCGGGAG CCGCCGCGCC CGGCCTCAGA CGTTTTTCTC TAGGTAAAGC 120
CGCGGGATGA ACCAGCCCCT GTGGAAATTT AGAAGTAACG ACGTCCGTCA ATTTCTGTAT 180
GAAAAATATA CAGATCGTGT GACACGTCTT CTGGGAATGA AAGTCTGCTA AACTCGCCGT 240
CACGAGTAGA TGAACACATT TAAAGTTTGT AGTTAAGAGG AAAACAACGC CAACGACACA 300
AATGCCCCAA GCGCTGGATG AAGCAGCGAC CTAGGATGGG GCTGGCCTGG AACGGGAACC 360
AAGACGCCCG CCCGGACGAA AACGAGCAGG GAAACCCGGG CCGGGGTCGG CCGCCCCACA 420
CGACGCACTG CGCAGAGACC ACGCGGCTCC GGGTCTCGCC TGCGCCGGCG CATCCCTCGC 480
AGACGCGCTC CTCCCACGCG AGGGCCCCTT CCCCGAAGCG CACGCCTAAG ACTGCGCGCC 540
GCAGCCCGCC CTGTCTAGCT GAGGCGCAGA CCCGGATGGG TCCCAGAGGG GCGGGTCGGG 600
GCGGAGAGCC GCGCCCAAAG GCAATGGGAG CCGCACGCTG CTAGGCAACA TGCTGTCTCC 660
CGGCAACGTA GAGGCGGGGA ATTCGCCAAC GTGTCTGAAA CAGACAACAA TTTTAGCCAA 720
CGGCTGCGTG GGCCTTGGGC GTCCTGGCCA ATGGGAATAG TGAGGGGCCT GTCACTAAGA 780
AACCTGTCCC TGAGCAACGC ATAGGAGGGG TGGAACCCAG CAGCGCTGAC TGAGCCGCCG 840
CGAAGTGCCG GAACGTATTA CCTGGGAGCC AAATTTCAGA GCGTCGTTTG TCTTCCCAAG 900
CCCACCAGCT TTCAGCGTTC TCCAGCCTCG CCACACCCCC GCCTCGGGCC GTCCCCGCCC 960
AGACGCTTGT CCCCGCGAGA AGCTGAGCGC ACTGAAGTGA GCCCGGCGGC TGCCGCCGGA 1020
GGAGGAGCCC GGCTCTGGAC ACGGCCGTCA GGAAGCTCAG AGGCTGCAGC ACCGCTTCTG 1080
CGTTGATTTC CGCTTGACTT TTACTCTTTT CTTGGGTTAA AAATCAAACG CCGACCCGAG 1140
GCGTCAGAGA TGGGCGGTCG TTAGGCGCAG TGGCGGCCCC CGGATGTTTG CGATGGGACG 1200
GCGGGCTCGG AACGTGTGGA CGTGGGCTTT GGAGGTGCGA GCCCCATTGG GCCAGGGCTG 1260
GGTCCGGGCA GTGGTACGGG GTCTCAGCTG TCCGTCACAG GAGATGTGCA GGCCTCGTCA 1320
TCTGGGGTCT TACGTGTCAG TGATGTGGGG TCTGCCGGGT CAGTGAGGGG GTCTGTGAGG 1380
TCACTAGTGG GAGGCCACTC CCAAAGTGAT TCCCCTCTGT CCCACCTGCT TCCCTGAGAA 1440
AAGCTCACTT ATCCTTCACC AGGATTTAAA AATATATATC CTAAGACCAA CCTGTAATAT 1500
TTTTTTCTTT TTTGGAGACA 1520
|
| |
|
|
|
