| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13525 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:76789060-76790890 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr17:76789684-76789694 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr17:76789684-76789694 | GTCACGTGAC | - | 6.02 | | MITF | MA0620.2 | chr17:76789680-76789698 | GCATGTCACGTGACCTGT | + | 7.24 | | MITF | MA0620.2 | chr17:76789680-76789698 | GCATGTCACGTGACCTGT | - | 7.24 | | USF1 | MA0093.2 | chr17:76789684-76789695 | GTCACGTGACC | + | 6.14 | | USF2 | MA0526.2 | chr17:76789682-76789698 | ATGTCACGTGACCTGT | - | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_62236 | chr17:76690401-76817069 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 76789581 | 76789839 | | chr17 | 76789842 | 76790846 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I078793 | chr17 | 76789661 | 76789810 |
|
Enhancer Sequence | GTGCTGGGAT TACAGGTGTG AGCCACCGCG CCCGCCCCCC TCACCCCCCC AGGAAGGCTT 60
TAAATGCTGA TGCCTAAGCC TCACCCATAG ATTCTGATTC TACTTCCGTC AGTATCGAAT 120
GCCTCTCCCC AGGTGCTCCT GCTGCCCTAT GAGCATTGAG AACCCTGAGG TAAGAAGGAG 180
AAGAGAACAG AGGGAGAGGA GCTGGTTTTA GCTTTGGTTT CCCCATGTTG TTTAATTTTG 240
GGGTGGGATG GGAATTCTTG AGGTAGCCTT GGAAGTCACT TACCAAGAGT AGTGGGCACA 300
TATGCAATGA GAGAGCAAAA TAGTGTGCAG GGATCACTGA AAAGAATGGG AGAGAGAGGA 360
AGGAGTTGCC TGAAGACCAA GGGCAGAAAT CCCAAAAGGC AGGCAGAGCC CAACGAAGAA 420
GGGCAGCCAG ACAGCCCTGA AAGCCGAATC CATGGCACCC AGATGATCTT CTCCAAGGGT 480
CATCCCCAGT CCAGATATGG AAGGAGCAGG GGGCCAAGCC AAGGCGGGAT CTGCACGAAG 540
CAGCAGCAGG GCCACCTCCG GGCAAGAGTG TGACTCCAGG GAGTCAGCTC AGCTGACAAG 600
ACACAGAAAG CTGCCCGTCT GCATGTCACG TGACCTGTCC ACACACAGTC CTCCTTTACC 660
ACCACGTCCT TGGCGTACCC ACATCCTCAT TGCGCTGAGG TTGTCCAAGC TACCAAGACT 720
TGAGGCAGGG ATTCTCACAG CACCGTCCAG TGTTAAACTG CCCTTAAGGT CACTATTACA 780
GTTATGATGA GCCCTAACAG TATGTTAGGG ATAAACAGAT GCCCACCTGA TTCCCCAGTG 840
TCCAGACACC TGGGCTTTTT CCTAACTAGA AGACTCGGAG TTCACCCACT GCCTACTTCC 900
CATGCCTAGG ATTCTCCCTG GGTTCCCTGT ACTGGTAAGA TGCCAACACG TCCACTAAGT 960
CAGATTGAAT CTCTCACCAC CTGAAGGCCT TCCTGAAACC ATCGGTGAGC CGCTTGCTTC 1020
CCTGGCTACT ACTTGGCCTC CGAACCCAAC TAACCACCCT AGCAGAAATC ATCTTAAACT 1080
CCACCCAGAA CATTCCACCC TATCTGTCAT CTCACCTCTT GAGTCCATCT CCTAAATATC 1140
CAAGTGACCT CACTTCTAGC CTATGCTACT AATGCCAATC TCTTAGCTCT AGCCTTGGCC 1200
ACTTCTCAGC CAACCTGGCG GCTGGTCATG CTCACCTGCT GTTCTCTGCA CTCCACCAGC 1260
CGCCTTTCAG GCCATCAGGC AGCCTGGAAT CCACTATCAG CCTCAGGAGT CTAAAAAGCA 1320
CATCAGACCT TGGTAACCCT TCTTGTCCAA ACTGTCAAAC AAAACCTGCC CTGCGCTTTT 1380
GCACCTGACT TACAGTTAGC CAGCTGAGTC CTGCTGGCCA GCTCCCACTG CCAGCCCCCT 1440
TTCAGAATGT CACCTCACCC CACGGTGCTT CAGGCAGAGC TCATGACAGG CTCCTCATGG 1500
CCTCCCTGCA TCTCCCTAAC AGCACTCACC CTGCCCTGGA GCCGTCAGTC CTGCCGGTGG 1560
GACTCTGCCC GCCGCCTGCG AGACGACGTG AGTGTGTTCA CTTTTATACA CACCCAGAAG 1620
TGGCCCTAGT GTTTGGGAAA CGGCAGTTAA GAATGGAAAA GCCTGTCAGG CGCGGTGGCT 1680
CACACTTGGA ATCCCAGCAC TTTGGGAGGC CAAGACGGGC AGATCACGAG GTCAAGAGAT 1740
GGAGATCAGC CAGGCGCAGT GGCTCACGCC TGGAATCCCA GCACTTTGGG AGGCTGAGGC 1800
AAGCGGATCA CAAGGTCAGG AGTTAAGAGA 1830
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