| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10971 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:9145940-9147420 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:9146646-9146661 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr16:9146643-9146661 | TCTTGAACTTCTGACCTC | - | 6.88 |
|
| | 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 |
| GH16I009052 | chr16 | 9146584 | 9147670 |
|
Enhancer Sequence | TTACAGGCAC ATGCCATCAT GCCCGGCTAA TTTTGTGTAT TTTCAGTAGA GACGGGGTTT 60
CACCATGTTG GCCGGGCTGA TCTCGAACTC CTGACCTCTA GTGATCTGCC CGCCTCAGCC 120
TCTCAAAGTG CTGGGATTAC AGGAATGAGC CACCATGTCC AGCTCTTTCC ATATGCTATG 180
AAAGCTCCAC CTCCCTTTTT CTTTTTCTTT TCTTTTTTTT AATTCAGACA GGGTCTTGCT 240
CTGTTGCCCA CACTGGAGTG CAGTGGAGTC ATCTCAGCTC ACTGTAGCCT CTGCTTCCTG 300
GGCTCAAGTG ATCCTCCCAC CTCAGCCTCC CGAGTAGCTG GGACCACAGG CGCATGCCAC 360
CATGCCCGGC TAGTTTTTGT ATTGTTTTGT AGAGATATGG TCTCCCCATG TTGCCCAGGC 420
TGGGCTCAAG CAATCCTCCT GCCTCAACTT CCCAAAGTGC TGAGATTACA GACGTGAGCC 480
ACCACGCCCA ACGAAGCTCA GATTTTTTTG ATTTTTTTTT TTTTTTTTTT TCTGCCCAGG 540
CTGGAGTGCA ATGGCGCTAT CTCATTGCAA CCTCTACCTC CCAGGTTCAA GCCATTCTCC 600
TGCATCAGCC TCCCAAGGAG CTGGGATTAC AGGCGTCCAC CACCACACCT GGCTAATCTG 660
TATTTTTAGT AGGGATGGCG TTTCCCCATG TTGGTCAGGC TGGTCTTGAA CTTCTGACCT 720
CAGGTTATCC GCCTGCCTCG GCCTCCCAAA GCGCTGGGAT TAGAGGCGTG TGCTCCCGCG 780
CCCGGCCCTG AGCTCAACTT TTTAAGGTGG ATTTGATATA ACGGCTGTGT ATTACTTAAG 840
AGAACACGAG CCACCGTAAC AAAGAAACCC TCAAAAGGAC AAAAAAAACA AAAACAAAAA 900
CAAAAAACCC GAAAATAAAC CCCCAAATCT CAGTGGCCTA ACACAAGGAG AATTTATTTC 960
TTGCTCATAT AAAGTCCAAA ACTGGTATTC CTGATAGGCA GGTGGCTCTC TTCCATTACC 1020
TGATCCAGGG ACCCACGCTC CTGCTTGCTC GGGGCTCTGC TTTCTCCATC AGGATGAGTA 1080
AAATGCAGGA GCACGGAGGT CAGCCCAGGA GGTGGTTACT AGCAAGGCCA CTAGCACGGG 1140
GTTGGGGGAA TGCCTCTCCT TGCATTCCTT TGGCCCAAAT CCAGTCACGT GCCCACCCTC 1200
AACAGCAAGG GATGCTGGGA AATGTAGTCC AGCCACAAGC CAAGGAGGTG GCCAGGAACA 1260
GCCTTTGGCC AACTCGGAGG CCCTGAGTGA TCTGAGTCTG AGCTCACACC ACCTTCCTCA 1320
TTCACTACGC TGTAGGTACA TTGATTCCTA TAGTTCCCCC AAATGAAAAC CTCTTTCCTA 1380
CCTCAGCTTT TGCCCGGGCT ATTCCTTCTG CCTAAAATGC CCTCCTCCTC TGTCCACCTG 1440
GCTGGTTCCT TGCCATCCTT CAGGTCTCAG CATGGGGATC 1480
|
