| Tag | Content |
|---|
EnhancerAtlas ID | HS133-30040 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:155142050-155143200 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr7:155142368-155142379 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr7:155142368-155142378 | GCCCCGCCCC | + | 6.02 | | Nr5a2 | MA0505.1 | chr7:155142562-155142577 | AAGCTCAAGGCCACT | + | 6.24 | | SP3 | MA0746.2 | chr7:155142367-155142380 | GGCCCCGCCCCCC | + | 6.11 | | SP4 | MA0685.1 | chr7:155142365-155142382 | CCGGCCCCGCCCCCCTC | + | 6.03 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59265 | chr7:155132785-155156935 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 155142108 | 155142665 | | chr7 | 155142200 | 155142600 |
|
Enhancer Sequence | ACAGGGCCAA AACTCTCGGT GCCTGTGGGA GGAGATGACG ACGCTCATTC TTGCCTCGTC 60
CTGCCACCGG GCACCACACT TTGCCCTTTG TAGGCAATGA CAGACCTGGG AGGTGGAGAG 120
AGCAGGAGAG CCACGGAGTC TGGAGCCAGC CACCAAAACT GCTGAGAAGC GAAGGAGGGA 180
CTCTGGAAGG CAAGGCATGA GTGTCCTTCA CACAGCCTGC AGATCTCCTT TCACCACCTC 240
CGTCCTGGAG GCTTCCTCCG CGTCGTCCTG GGGTTCTCCT GCCTTGGAAA CCCAGCTGCT 300
CCCCATGCAG CGTAGCCGGC CCCGCCCCCC TCCCGCAGGA AGCTCAGAGA GGGTGCAGAG 360
ACCTCGCAAG TGCAGGCTCG GCCATCATCG GAGCTCCACC AGTAGGGTCA AGGAGTACGC 420
GGCTGGAGCA GGTTTCCAGC CCGGAAGGCA TTTCCCTGAA ATGTTTGAAG ACGCCGCTGC 480
ACAGGCTTCT GACCTGCAGT GTCGCTGTGC GGAAGCTCAA GGCCACTTCA GGGCCGGAGC 540
AAGACTTTGG GGTTCTTCAC CCCGCGTGTG CTGGGCCTCA CTCAGTGGGT AGACTTTCCC 600
CGAATCCCCA CTTTCAGCCT GGGCCCTACC CTGAACCCCG GTCCCGTGAC TGCTGCTCCC 660
AGGACAGAGC GTTTCTGGTT CAATTTCTCC CGAAACCAAT GCCCTCGTCG TCGGCCGGAG 720
CAGGGTTGGA AGACCATGCC AGCGCCTAAC TGCTCCCCGA AAGACGTCCA GCCACTCTTC 780
CTCTTCCCTC TCATGCTGTC CCTCGGGGGT CTCGGGTCCC AGTTTCCCGG CCTGCTGGGC 840
TCACACACTC CCTCGGCTTC CTAGAGACCC GGCTTCCGGC TTCCTGCGGT CTCCCGGGCC 900
GGCCTCCCCT CCCGGCTTCC TGAGGTCTCC CCGGCCGGCC TCCCCTCCCG GCTTCCTGCG 960
GTCTCCCCGG CCGGCCTCCC CTCCCGGCTT CCTGAGGTCT CCCCGGCCGG CCTCCCCTCC 1020
CGGCTTCCTG AGGTCTCCCC GGCCGGCCTC CCCTCCCGGC TTCCTGAGGT CTCCCCGGCC 1080
GGCCTCCCCT CCCGGCTTCC TGAGGTCTCC CGGACCGGCC TCCCCTCCCG GCTTCCTGAG 1140
GTCTCCCCAG 1150
|
