| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13000 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr17:58211500-58213930 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr17:58211664-58211679 | GATTTCCTGAGAACT | + | 7.99 | | ZNF263 | MA0528.1 | chr17:58211975-58211996 | GCCCCCTCCTCCCCCACCCCC | - | 6.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAAGTTAGA AAGGAAAGAG GTTTAATTAA CTCACAATTC TGCATGACTA GGGAGGTCTC 60
AGGAAACTTA CAATCACGGC AGAAGTGGAA GCAAGGCACC TCTTTCACAA AGCAGCAGAA 120
AGAAGTGTGG AGTGATGGGG GAAGAGCCCC TTATAAAACC ATCTGATTTC CTGAGAACTC 180
ACACACTATC ATGAGAACGG CATGGTGGAA ACCACCCCTA CGATTCAATT ACCTCCACCA 240
GGTCTCTCCT TTGACACGTG GGGATTATGG GGATTACAAT TTAAGATGAG ACTTGGGTGG 300
GGACACAAAG CACCTAACCA TATCAGCCCT AAAGCCATGG CTGGAGAAGG CTCCTGCCAG 360
AAGTCCACCC CGAAGCCCTC AGACTCCACT GTGGCCTTTC CTCACTCTGC TTCCTATCTC 420
CATTTTTCTT TCCCTGAAGG AGGTTGCTCT ATCAATGCCT CCCGTGACAA CACATGCCCC 480
CTCCTCCCCC ACCCCCCAGG CTCAGCGATA AGGAAGCTGG TGCCCTGAAT CCCTGCCCCA 540
CCCAAGACTC TTTCCTTTTC TTCCCACTTA GTCTACTTGA AACTCCTCTC TGTATTTTTT 600
TAATTAAGTT ACCCACCTCA GCTTTGTTTC TCAAAGGCTT TAACTTTTCC GGGAAGAGCT 660
GCAATCGTTT CTTGGCAGGA GTAGTTTCAG GTTTGCATTG CTCTGAAAGA GACTCTCAGA 720
AACACGGGAC CTCCATTTTG GTGTCAGCAC CGCACGCACC CCCACCCAAG CCAGCACCGT 780
GGCTGGAAAG CTTACGTATA GGATAAGGGA TGTGGGTGGA GTGGGAATTG ACGTGGAGGA 840
TGTTGGAGAT CAGATCAACA GATGCTACAA AAAAACCCAA CCCCTCCCCA CCGAAAGACG 900
GCAATACTCA GGCTAGGAGC CGCTGCACTA GGTGCTAGGG ACCCACTGAA TTTTCACCAG 960
AGCAGTGGCT TGGTCAGATC TCTATTTCCA GAAACATCGC CCTGGAATCC TTTCCTTGGC 1020
GTGGAAGGAG AAGTTGACCC CGAAGAGTTA CTCAGTCAAG GGCGACTCAT TGCTCCACTC 1080
TAAGGTTTCT CTAAGCACAG GGCGGTGGCG AAAGGGAAGG GCTGCAGGGT GGAGTCCGGC 1140
ACCAAGACCT CCCGGCCCGG CTTCTAGCAG CACACGGACG CTTGAGATGA TTTCTTCTGA 1200
AAACGGGCAG TGGTTGAAAA CCACTGCTTC AAAACACAGA CTGGAGGAGT GGTAAATACT 1260
AACGAGGAGT TTTAGCAATG GACTCTGTTA ACAGAGTCTG GTCGCCTGAG AAGGGCCTCG 1320
GAGGACTGGC CAGGTTGGAG AACGATTTCA ACTGCGTACT GGACGACACA CAGAAGACTG 1380
CGGGGAGCCT TAGCCCCTAC CCGGCCTGCA GTGCTCTCTG GGGCACACGG CAGCCCCACG 1440
ACGCCTTTGG GTTTCTTCGA GCGCTACTCG CACGCACCAG CGCCCACACA GCTGCAACGC 1500
CAAACGCCCG CCAGCACCTT AGGGCCGCGG GAGTCCCTTC CCCAGGCCCG CCCCACACGC 1560
CGGCCTTTTC TGCCGCTTCC CAAGCCGGAG CCAATCAGCG CTCAGCAGCG ACCGGCAGGG 1620
ACGACCAATC GACTTATCCT GCGTTGTGCT AAAGACCTAG AAATCGAGCG TGGTACATTC 1680
GATCGACGGA ACGTCTGGGC CCTAGTGCTA AGTTGGGTGA CTGTTCGGTG GTTGTCTCGG 1740
GGGGTTGCAG GAAGATCCTG TTTCCTTGGC GTAGAAGGAG AGGTTGACCC CGAAGAGTTA 1800
AGATTCTCGA AGCACACTAT TTATCCGTGG CCCTCCTCCT CCTTCGCGGG GTAGCTTGGG 1860
GCAAGTCATC TATTCTCTCT AGATCTGTGT TCTGCCTAAA AATTAATGAA TGGGACAAAA 1920
TGGTCTCTAC AGTCCCTTGT TTATCCTGGC CCTGCAAATC CAGGATCGCT GCCGTTGTAT 1980
CTCAGTCTGA TGTCGGTGGT CTTGCGCTGG CCGGTGTTCT GAAACTTTGT CGGCAGTAAC 2040
ATGCACTCCA GTCAGTCTCT TCAGTCCAGG ACACCATCGC CGGGGAAACT GAGGCATAAG 2100
AAAAATAAAA ATGAGCATTG TCCATCCACA AATATGTATT GTGCTCCCGT TGTGTATCTG 2160
GCACTGCCCT GGTGCTGGGT CCCCTATGAG AAACAGGCAT GGTCCTTGTG CCCCTAGTTA 2220
TAAACTATGT CACTTCCATC AGACTCTGAG ATCCCCAGGG AGGAGCTGTA CTCTCATCAA 2280
GCTGCTCTCA TCAGCAGACA GGAAGGAGAC AGACTTGTAG GCCTGCATGC TCCTGTGCTC 2340
CTCTTGAACT CCCAGCTCAG CCACTGGCTG CCTTTTACCC ACAGATCTGA AAGGAGCCAG 2400
GGCGGACAGG CTCCAGCAGT ACCTCTTTTC 2430
|
| |
|
|
|
