| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10047 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:51369050-51370230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr15:51369286-51369297 | TCCTTATCTGT | + | 6.14 | | Nr5a2 | MA0505.1 | chr15:51369554-51369569 | AACCTCAAGGCCAGC | + | 6.23 | | RUNX1 | MA0002.2 | chr15:51369476-51369487 | AAACCACAGAC | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38708 | chr15:51368827-51370432 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I051075 | chr15 | 51368081 | 51370530 |
|
Enhancer Sequence | TTTGCTTTCT CAATTTAATA GTAACCCCTT AAGTATGATA AATTGAATTT TTGTCATCAT 60
CTGGGCACGC ATCAGATGTG CGCTGATGCC TGTGGAGAGG TCCTCCGCGT TCCTCCTCTC 120
CCGTGCTGGA TTCCTGCCGC CCCCCATTCT ACTCCCGCCA TTCTTCGTAA ATGGAATCCT 180
CCTGCTTCTT TCTCACTGTG TAACACCTGG GGCATCGACC TTGGAGCCTC CAGCTTTCCT 240
TATCTGTGAC TTCCCTCCAA AATGCTGCTC CCTCCCCTGT TTCCCTGGGG CCCTTGACTC 300
CTCCATTAGA CCTCAGCCTC CTCTGTCAGT CCTTGGCCTG TGCTCGCCAC AGAGCGTGCG 360
GTCAGCAGGC GTCATGCTGG CTCTCCCCAA GGCCTCTTCC TGTGTTGGCC TCAGTGCCCA 420
CAGACCAAAC CACAGACTGC CAGGCCCCCA GGCCCCGGCA GGCCGCCCTG TGCTGACGTA 480
GCTGTGGGTG GGACTCGTGT CCGAAACCTC AAGGCCAGCC CTTCCCGCTG GTCCCATATC 540
CCAGCTGCCC CGCCTGTCTC CCCAGCCTCT CATCCCGCTT TGCTCAGCGC AGCTCCTCCC 600
TAAGCCAAGC ACGCCCTGCT GCCCACCCCG CTCCCATCTT ATGCAAGGGG GCCTAGTCAA 660
GGAACCCCCA CCTGGCTTCA ATTGTTTGTA CCCTGGCAGT TCCGAGAGGG GAGACCTTTG 720
ATAGAGACAG GAGACAGCCA AGGGGTCCCT TGCAAAACAC CCCATTCAAG CCTAAAACAG 780
TCTGAAAGCT GAAAGACCCG ACTGCCGGTC CCGTAAGAAA CCCGCAACCC AGAGGGAGAA 840
CACCCTTGTC TGCCCTCCCT TCCCCGACAG CTTCTCGCTT AATAATATGC ACATGCGCAC 900
TGGGGGAACA GGGGGCGGAG CCTCAGGATT TCGCGCCTTG GGCAGGGGGA GGAGCCTGGA 960
CTCCAGCTCG AGTGTGCTGG CCTGGAATTC AGTCTGTGAG GTGGAAGCCT GTTAGCAGGA 1020
CCACTTATTT TTTTCTCCGA GAGCTTTCTT TTAATAAATT CTGCTCCCCT CACCTTTCAA 1080
TGTGTCTGCG GACCTCATCT TTCCTGGTCA TGTGACAAGA ACCCCGTTTT AGCTGAACTA 1140
AGGGGCAAAA ACTTCTGCAT CACCTTAACT GTCGTGTTCA 1180
|
