| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21781 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:46910070-46911760 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | + | 6.01 | | MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | - | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26636 | chr22:46909700-46911877 | Esophagus | | SE_34191 | chr22:46909995-46911887 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46910107 | 46911726 | | chr22 | 46910355 | 46911003 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046513 | chr22 | 46909817 | 46911837 |
|
Enhancer Sequence | TGGGGTCAGA ATCATCTGAC CTTGACTGTG GGTCTTTCCC ACCCAGGTAG GCTCCAACAC 60
CAGGGGAATC CCACCCAGTC CTCGAGATGA CAGTGTCAAA AACCCAGTAA GCGAGACTAC 120
TCACAATGGA GCCGGCATTT CTGAAGGGTG ATTATTTAAG CCACACCTCA ACTGCGGGCC 180
TATGTGATGC TGAAGCTCTT CCACCCAGAC GTTTCACCAG GCCCCGACGG TCCATCCAGG 240
TGAGGGCTGG AGTCAGGTCC ACCTGCACTC TGATCCCCGG GGGCCCAAGG CCACACACCT 300
CTGGCTGCCA GTCAGTCAGA ACCAGTCCTG GTGAGGTGGG GAGTGGGGGC ATGAAGGATG 360
TGGCCTGAGG ACACCCCAAC AGCATCTGTG TATCACCGCC AGACCCTTGC TGAAAGTCAG 420
GGATAATGCA ATGGCCCCTC TCAGCACCTC CCCAGACCTC CCCAGACTCT GTGGTCCCTC 480
CTCCCAGCAT CAAAGAGAAG AGTCACTCCC CGGAGGGAGC CGGGGCTGCA GGGCCGAGGC 540
TCACGGCTGG GCTCTGGAAT AAGAGGGGTG TTTCTGAATG AATTGCCCAG CCCTGTCCTG 600
CCTCGCTGAG TCATTCCCAA GTCAGCAAGC ACAAGTCACT GCGGGAAAAG CTCTGGAGCT 660
GCCACCCCTT CCCACCCCAG GGATGCCTGT CCGTACCCGC CGTCAATCCA GCCCTCAGGC 720
CTGGGGGATG AGCACCTCAG ACGTGCTCTT TGCAGCTGGC ATCCGCTCCA AACTCCATGC 780
CTCCCCACAA AAGTGGCTCT GTCCAAACCC CAGCCCTCTT GGGCCCTGGC AACCAGCCTA 840
GTCCTCGCCA GCCCCTTCTA GAAAGCACCC CCAGCACCCC CTCAGCTTCA GCCTGGGCTG 900
AGAAAAGGCT GTCTGGCAGC GTGGACCCCC CTCAGCGTCC CAGCAGAGCC AACCCCCCCC 960
GGGGACACTC ATGGGACACA GCATGGGCAG TAGGAGCCAT TCCACCCGTG CATCAGCCCT 1020
CTGGCCACAC TCTGGGACCT CATGGCCCTG CCCACCACTC CCAGCCCACA GCCAGGCAAG 1080
TGACCCCCAC CTGGGCCCTC CTGGGGAGAG CTGCACAGCT GTCGGCAGCA CAGCTGGAAC 1140
CACAGCCCAG CGGTCTCAGT GCGTATCACA AAGGCTAGCT TGTGAGTGGA TGCTCCCAAG 1200
TCACATGACC CCCAGGTAGG AAGGTTTGCA CATGTTTCAT CAGGGTAAAG GGAAAGAGGC 1260
TCACCTTAAA CACAAACTCT ATGAAGGCCT TAGACAGAAA ATAGGAAAGC ATGACAGTCT 1320
GTGTCTCCAT GGTGAAGTCA GCTCTGGGAG GGCTGAGCCT GATGCAGAGT GGGTGTGCAC 1380
AAGCTGCAGG GCACCCCGGG GGCTGGAGGT GGAGGACACA GCCAATAGGA CGGGCCTCAG 1440
TCACACAGTG CTCAGGGCTG GGGACTCAAA GGCACAGAGG CTGAGGCTTT GTAAGTCCTG 1500
CTGGGGGATC AGGGGATGAC TAAGTCACTG GGGCCTCCCC AGCCTGGCAG GCTCCTATCT 1560
GTGTAACAGG CTCCCAGCAG CCAGTGTAGG AAGGCAGCCC CGGCAGGAGG ATACACCAGG 1620
ACATTCCGCC CATCCTGCAG ATCTCCAGCA CTGACCAGCA TCCACAGCAC AGTCGACTGG 1680
GGTTAAGAAA 1690
|
