| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00331 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:11763380-11765160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:11763418-11763439 | AGATGAGGGAGAGGGGGAGAG | + | 6.76 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68783 | chr1:11763666-11765945 | H9 |
|
| | 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 |
| GH01I011704 | chr1 | 11764421 | 11764550 |
|
Enhancer Sequence | GTTGAGTCCC AAAGGATGGG CAGGACGTGG ACGGAGAGAG ATGAGGGAGA GGGGGAGAGG 60
TTCCATGCAG AGGGGACAGG CAAAGTGAGA ACAGAGAGCC AGAAAGCAGG GGTGTGTTTG 120
GGGCCCAGGG AGCAGTCTCT GTTGCCTGTG AAGGGGAGAA AGTAGAAGTT GGAGCTGCAA 180
AGCTTGGTTG GGGCCACATT ACACAAGGTC TTCAGTGCCA AAGTAAGGAG TCTGTGGTTG 240
CATGGGAAGG CAATAGGGAG CCATAGACAG TTTTGAGCAG ATAAGGGTCA CAACCCGAGT 300
AGCCATACCA CCAGTATATG CTGGGTCTGG GGACAGGATG GAGCCCCCTT GGATGCACCC 360
CCATGGGTGC TCTGGCACTG TGCACTGAAA TCCCACTTCC TCTGTCCCAG GCTGGCTGCG 420
TGGGTGATAT GTGGTTCTTG AAGGGTGGGA GGGAACAAAG ATGGCATTCA GACTGGGGTT 480
CCACTGGCCC TGAAGCAGGA TGGGTACTGT GAATGGACCC ACAGCCAAGT AGGGTCGTGG 540
CAACGGAGCT TGGGAAGGTG GCAGTCTGGG TGGGATCATG CTGCTTCGGG GTGTTGGAGT 600
GGGGCAGGAG TGGGAGTTCA TCTCCTGGCT CTGCAGGGAA GGAGCTGTCC TCCAAGACCA 660
GCACCTAGGC TGCTCACCAG GCTCAGAGGC GGCTCTGAGG TTTACTGACA GCCTTGTGTG 720
TCCCCAGGGA CAGCAGACTA GCTGAGAAGC TGCCCACCTC TCTACTGAGC CTCCTCTGCT 780
CTCTTGCCCG CACTGTCTGG GTTTTCTTCC TCATTCCCCT CAACCCCCAG GACAAGGAGG 840
AGGTGGTGAT TCCTTTCATT GGCCAACGTC CCGAGGTTTC CCTGTCCCTA GGACGCTCTT 900
CGGGCTTCTC CCAGGCTGTC ATGTCCCTGC AGGACAGAAA GGCAGGGCTG GGTCTCGGAC 960
ATGGACGGGA TCCCATATGC GCTTGGCCTT TCCAGTCACA AGGAGAGCAG GGGGTGAAGT 1020
CTGGCAGTGG TCAGGCTAAA TGCCAGCCCA GAGAGCAGCC CCGCTCCACT GGCCCCGAAG 1080
CAGGATTGAG GTTCCCTCTG CGCCGAACAA TGCTTGAGTG ACAGGCCTTT AAAATGGGCC 1140
CCTCCTCCCC CTGGGCTGCC TCAGGAACCA GGGACACAGG TCCCGCTTGC TGAGCTCTGG 1200
CCTCAAGAGC ACTTGTTAGG GAAGGGCTGG AGGCAAGGCC AGTGGGACAG AGCCTTCCGT 1260
TGCTGGTGAC GTGACCAGGA CAGTAGCAGG GACTGTGGTG CAGGGTCTGT GGCCTTAGGA 1320
ATGGATGCAG GTGTGATGGG AGACAGGGTT GTCACAACAA GCCTGTCCCA GGGTCCCACG 1380
CACGTCACCA AGGCTCACCT AGTATCTTCA GCCAGATCCC CGGGATAGGG GACAAGATGG 1440
AAAGTGACGG CCACCTCCTT GTCTCCATCC ACAGTTCTAG GAAGAGCTGA GCTGTGGACA 1500
GTGGAGGCCA GGGCCCAGGA TCCCAGGGGA CCAGGACATG CCAGGCTGGG ATGGAGGCAG 1560
AACTGGGTGA AGCCACCACA GACCCTGCGA GGCTGGAGAA GGTGTTTCCC CCCTCCCCTC 1620
CACGAGTGCG TGGTCAGAGC TTCGAGGGCA CAGCAGTTTC CCTGCCCTAC CACCCTCCCT 1680
CGGGGTCGGG GCTAAGGTGA CACTGGGGTG GGCCAGCCAG CATGGGGGCC GCAGGGAGAG 1740
GCGCCGGGAA GCAGGGAAAC ATCACAGGCC CACCAACCTT 1780
|
