| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32485 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:138466940-138468850 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr9:138468661-138468672 | CCACACCCTCT | + | 6.02 | | NFKB1 | MA0105.4 | chr9:138467346-138467359 | TGGGGAATCCCCC | + | 6.13 | | NFKB1 | MA0105.4 | chr9:138467346-138467359 | TGGGGAATCCCCC | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr9:138467484-138467499 | GAGGTCAGGAGTTCA | + | 6.22 | | PLAG1 | MA0163.1 | chr9:138468463-138468477 | GCCCCTTTGGCCCC | - | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGAGCTT CGGGAGGGTG AGGTGGGCAC ACACAAGAGC CACTTCCCGG GCCACGGTCT 60
CCAGACCCTG GACCGGATGC CCAGCCTCAC ACCCGTCGCA CAGCAGTGAC CCAAACCCCG 120
GGGGACATCG TCAGCTGAAG GGTCCCCCTT GTGCCTTTGG TGGCGTCCCC TGGGTAGAGA 180
AGGGGGTGCC AAGCAGTGCC TGGGCAAACT CACTCCTGTA GGCAGAACTG GTGTCTCCAC 240
TGCGGGGTGA CTGCTCAGAG GCCAACGGGC ATCTTGGTGA GGTGAAGATC CCACCCCAGC 300
TCACCCAGCC TCTCCCAGGG CCAGGGTTTG GGGAGGTTTT TGTTGAGTAC CTTCATCTCC 360
CAGAGACAGC GTCTCCCCCT GGGGAGCTCA GGTTTGGTAG AAGCTGTGGG GAATCCCCCT 420
TTTCTGAGTT TTCATTTTGC AAGGGCAACA CATCGGGGGT CATATAAAAT CCATTCTTGG 480
CCGGGCACAG TGTTTCACGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG CAGGTGGATC 540
ACCTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTACTAA 600
AAATACAAAA ATTAGCTGGG CGTGGTGGCA CATGCCTGTA ATCCCAGCTA CCCGGGAGGC 660
TGAGGCAGGA GAATCACTGG AACCCGGGAG GCGGAGGCCT CCAGTCTAGT CAAAAAAAGC 720
AAGACTCAGT CTCAAAAACA ACCGAACAGC CAAACAAAAC CCCACAAGTT CTTGTCAAGA 780
TTAAATGACT TTTACAAGTT TGTGGCATTA TTAGAGAAAA GACTTAAGGG CGGCAAGTGC 840
CCAGACGTCT GGTCCTAACA TCCCCAGGGG TCGCCACGGC CTTGACTTCT TGAGACTTTT 900
GGGCCTCTGG TTGGGCTGAT GTGGCCTGGA CACAGGAGCT CCTGGTGCTC AGGCTGGTGG 960
ACCAGGCCCC CCGGCACCTG GGCCCCCACA GCTGTGTCCA GGATTCCTGC TCCACAGAGC 1020
CTCCCTCCCT TCTCTGAGAG CCGCTCGGCC TCTGGCCACA CTCTCCTCCC CCCGGGGCCT 1080
GAGGACCTCT CCCCACTGCC TCACCTGCAT TCCCACCTCC TCCATGGCCT CGGTCCCCTC 1140
CCCAGGTCTC AGGGACTCGC TCTTTCAACC CAATGCTCAT CTGTGGCTTT TGGGCCTGGG 1200
AAGTCCACAC CTGTGCCCCA GAGACGCCAC AGTCCAGCAG CGTGCGACCC AAGGGAGGCG 1260
GGAGCTTGCA CTGCGAGAAC AGACACGAGT GGCCAGGCCC AAGGCCTGCA TGCCCAGGGC 1320
GGGACTGACT GCTGCTTGCT TTGGGGAGAA TGCTGTCGAG TCTCATGCTC AGAGGCACCG 1380
GGGACAAGCA GGGGAAGGAA GCAGCGCTGG TCACCTGTGG GCTGTTCACA CGCAGCAGCC 1440
ATGGCTGTGG TCACAAGATG AGCTGGGCTC AGCCAGCGCC ACGGCATGTT GCTGACTCTT 1500
GACCGGTCGA CACGTGAGCT CTAGCCCCTT TGGCCCCTGG ATGTCTTCCT GTCTCATCCC 1560
CCAACATTAA GGTTTGCCCT GATCCTTCAG GCCTCACAAG AGGGCCCCTG TCCCAGCCTC 1620
TGGCCTGGCT CCCCTTCTGC TGACGGATGT GGGGCTATCA GGGACCAGGA CTCCTGACTG 1680
CCCCTTGAAT ATCTCTGTCT AGTTTGCTTT GCAACAAAAC CCCACACCCT CTTCCACTGC 1740
CATTTCTTTC TCTCTCTCTT TCTGTCCCTC TCTCTATCTC TCTCCCTCTC TGTCTCTCTT 1800
TGAGATGGGG TCTTACTCTG TCACCCAGGC TAGAGTGTCA CCCATGGCTC AAACATGGCT 1860
CTTTGCAGCC TCAAACTCCT GGGCTCCAGC AGCCCTCCTG CCTTAGTCTC 1910
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