| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17542 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr2:122456900-122457960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:122457521-122457542 | GAAGCAAGAGGGAGAGAAGGG | + | 6.5 |
| | | 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 |
| GH02I121698 | chr2 | 122456236 | 122459153 |
| Enhancer Sequence | AGAGGCTGAG GTGGGAGGAC GGTTTGAATC CTGGAGGTGG AGGCTGCAGT GAGCAGAGAT 60
GGTTCCACTG TACTCCAGCC TTGGCAACAG AGTGAGACCC TGTCTCAAAA AAATATGCAT 120
TTTAGGTATA TTTACCCCAC ACACACACAT ACAAATAGGC CAGTGCAAGA TGAGCCAGAA 180
GAGAGCTGCT TCGTTCAGTC TGAGTGACTA AGAGTGATGA TGCCATCCAC CCAGACAGGA 240
AGCAGACCGG GTGAGCGGGT TTGTGGGGAG AGATGAGGTC AGCTCTCAGA GGTGACAACG 300
CTCCTAATGA TCAAACCCTC AGTAGAGGCC CACTGTGCCC GCATGGGAGG TGCTTTGCCC 360
CCACCTCCCT CAGCCTTGCA AGGTGAAGGC TCTTGCTTTC ATTTCACAGG GAAGCTAACG 420
GTGTTTAGCC AGTATGACCC AGATTTGTCC AGCCCACTGT GCCTGTCTGG GTTCGGGTGC 480
TGAGGGCCAT TCCTTGTGAT GCGGCCAGCA AGCAAGGGGC GACCTGGAGC TGAGAGAGGA 540
GGTGAGAGTC AGAGGAGCTG CAACATTTCC TGCACTGAGA TCCTGGTAAA GCCACAGGCA 600
TGGCTTGGCC CCCGCAGGAA GGAAGCAAGA GGGAGAGAAG GGGGAAGCCC TACATGTAAG 660
ACACTCTCTC TACTGAGTCC TGCCGATCAC AGCAGCTCCT CCTGGAGAAA TGTCCACCCC 720
AGTGTCGCCA AGTTAAGACC TCGGCCTTGC TCAGCACCTG CCCAGCAGCT GATGCTAGGA 780
CCTCTGCCAA GCATGAGGAG AGGAGCCAGC TCAGAGTGAC TCATTGTACA TCAGCCTGGC 840
TCCATGGATC CGGATCAACG CCCTGGACCT CACCTGGCAG TGAGGAACCA GTGGGAAGAG 900
AGGTGCGTGC TGGACTCCAC TGGACAGCAC GTAGTCTCTC GGTGGAAGCA AAGACACCAG 960
CCTTGCACCG AGCCAGCCCA GCCAGGGAAG AGTGGAGAGG AGGCAAGGCT GGGGGCTGGT 1020
GGGTGACTGT GTAATTCCCA AGCCAGGTGA AAATCTGTAC 1060
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