| Tag | Content |
|---|
EnhancerAtlas ID | HS133-23571 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:195573860-195575100 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:195574688-195574699 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr3:195574686-195574697 | GGCCACACCCT | + | 6.32 | | NR2C2 | MA0504.1 | chr3:195574036-195574051 | TGACCCTTGCCCTCT | - | 6.39 | | ZNF263 | MA0528.1 | chr3:195574908-195574929 | TTTCACCCTCTCCCCTCCTCC | - | 6.31 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23816 | chr3:195573836-195575210 | Colon_Crypt_2 | | SE_24828 | chr3:195573792-195575265 | Colon_Crypt_3 |
|
| | 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 |
| GH03I195847 | chr3 | 195573980 | 195574341 |
|
Enhancer Sequence | CCAAGATCAG ACAAGGGGGC CGGGTGCGGT GGCTCATGAG TACTTACCGT GTACCTGTTA 60
CTTGCCAGGC TGTGGGTACA GGAGATAAAC CTGGTCTCTG CCCTCATGGA GCTTCCTGTC 120
TAGTGGGAAA TCTTTCCCCA GCTGTCTGGT GTCCACTCCC TCTGCCTGCC CACTTCTGAC 180
CCTTGCCCTC TTCCTCCCCC GCCCTGGGCC TCGCTCCTCT CTTGGCACCT ATGGGCAGAG 240
AAAGAGGTTG CCCAGGTTAT CAGCCACACC CCTTTGGGCT CCGTTTCCAT TTCGGAGTGT 300
GGCCTGGTCT CTGCTCTCCC CAGGGAGGTT TTGTGCATTA GTCACTCGGC TTGCGGAACA 360
TGGGTCAGCA GAGATGATGG GGTCACCAGG AGGACAAGGC TGCAGAGCAA GGACTTGCCC 420
CAGAGTCTCA CCGCCTCTGG GCCCCTCTGG AATGACCACG GCCAAGCCTG TCCTGGGGAG 480
AAAAGAAGGC ACAGGCCGGT GATGGGTCTA GCTGGGGCTG GCGCTAGGTG CGGGGCCCCA 540
CCGGTGACAT GCCTGATCTG TCCACACGCC CGGAGGAGGG CAGTCCCGGC TGTCCTGGGC 600
TGGCCTGCGC TGCCCCCTTC CCTCCTTTCC AGCCTGTCAC AAACCCTGGC ACTTCCTGCT 660
TGGTGCCTCG GTTCAGGCCT GGGTCTTGCT CCCTGGGACC AAGGAGGGGC TTCCTCCCTG 720
ATCACCCCCG CCCCGGACAC CACACCTTCG GTTCACCCTG TGCCCACCTC TGCAGACTCC 780
CAGGAGCAGC CCTGCACAGC GCCTCCCCCA CCTCCAAGCC GGACCAGGCC ACACCCTCCC 840
CAGTGCTTCT CCTGCTCATC CATGGACAAC GCTACAGGCC ACCGAGTTGG CCCCCACACC 900
CTTCCTGGGG GTGGGGGTAT CTTTATGAAA ATGGAGGGGA AATAGAGATG CTCTCAGCAT 960
AACAGTGCAC CAGAGTCGTG AGGCCACCAA TGATGGCAAA AGAAAGGTGC GCTGGTTTTG 1020
TGGCTGTGCC TTTCCGAGGG CCATTTTCTT TCACCCTCTC CCCTCCTCCA TGGCTCCTAA 1080
AGTCTTCTCG TCTGCTCCAG GAAGAGGAAG ATTGGACGGA GCCAAGGTCC TGGGTGGATA 1140
GAAGGGCCTC CAGGACCCCC TGGATGTGGA GGAGGGAGGG AAAAGCTAGG GTAGAGCAGA 1200
AAGAATCCCC AGTGTCCCCA TCCTGGGCGA AGGCGGCTCT 1240
|
