| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10470 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:81384280-81385770 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr15:81384540-81384560 | GTTGGGCACGATGACCCAGA | + | 6.09 | | ZNF263 | MA0528.1 | chr15:81384935-81384956 | GAAGGAAGAAGGAAAGAAGGA | + | 7.03 |
|
| | 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 |
| GH15I081091 | chr15 | 81384221 | 81385795 |
|
Enhancer Sequence | TTCTGAATGG CCCATACTTC AAAAGGGAAA CAATAAATCC TCCGGCTAAA GCCCTAACCT 60
TTAGAGGGTG ATGTCAGAAG GAACACCGGA GACTGGACGC CGGAAGACCT GGGTGCTAGA 120
CCTGGCTCTG CTGGCCTTTC ATGATGGGGA ATTCTGTTTT CCTCTTTACC CCTGCTTTGT 180
GTATCACTCA AGGAGTTTTA CGAGGAGATC GCTAAGCTCT GACATTGCGA GACACCTTGT 240
CCCTACTTTC TGAGACAGAG GTTGGGCACG ATGACCCAGA GGTGAGAGTT GATTTGGTGA 300
TTCTTGTGAT CTGAATCTCT TCCATATGTC TAGTGTCAGC CCAGCTCAGG GAGCAGAGAA 360
CACGGGCAAT CTGATACCTC CAGGAAGTCC AATGCTTCGT TGTTGCTAAA ATTAGAACCA 420
GGCTGCAGCT TAGATCAAGG CCATTCCTTT CCCAGCCTCA CGGTGAGCTA ACTCTTCTCC 480
CTCCACCCTG CACCGTACAA ATGTGCCGGT AATTATAGCA ACATGAGCAC CAGATGATTC 540
ATCTTGGAGT CTGGAGGAAA AAAGCAGAAA CCAAGTTAGA GCTTTACAGA GATCCTGACC 600
CTTATAGACA AGGAGATGAG AGTAGGCAAA AGGAGAAAAC AAATGAGACA AGAGGGAAGG 660
AAGAAGGAAA GAAGGAGGCA GAAACAATTG AAGAGAATTA ACTTCTTAGC CTGGACAGGA 720
ACATGAGCGG AAGACCTAGT TAGTTCCTAC TTACCCTTTG CGGCTGTGTT GGCAGCGTAC 780
CAAATGACTT CCCCAAGGAC AGTGGTCCAT TCTTTTTTGA AAAATAACTT CAAAAAATGA 840
AATCATGATC TTTCCTGGTA ATGCATTTCA GTAGCTTGCT TGTATCTGTG TGTCAGTACG 900
AATGGAGCTG GAGCTAGGCT TGATCCCAGC TTTGATACAG ATTAACCATG ATCTCGAGCA 960
ATTTACCTAA TTGTTTGCAC CTCATTTTCT TTGTCATAAA ACAGAGAGAT CTACCTCAAA 1020
GCACGCTGCG CAGCTAAAAT AAGGTCAAAT ATATGAGACT GCCTGGAAGG TTCACACAGG 1080
TTGGCCCAAC CTAGGTTTAG CTGAAAACAT ATGTAAAAAA GATTGTCTAA TCTAGGTGGT 1140
CTTTGTTTCT GCCTCTGGGG ATCTTAATTT ATCATAGGTA TCCATTTCTG AGGTTGTTCT 1200
GTGGTAGTTT CTTTATCCTA TATTTCTCTA ATCATCCACT AGGTTTGCAT GCAGATGGCA 1260
AGACTAAAAG TTCCTTTCCC TTCTGGTTGA CAATGGAGTG GCAGTTAGCT TTTTAGGAGC 1320
TACCCTATCT TGAGCCTGTG CTGTCCAAGC TCTCTGTGCC ATTTCTTCTG CTGTACGAGG 1380
GGATAGATCT GTCCTGCAGG GCTGTTGTGG AGATTAAAAG CAATATCAAA TGTGAAGTGC 1440
CTAATATAGT GGTAGATACA TAATAGATGC TTAGGATGAG AAATGTTTAA 1490
|
