| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01605 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:46985550-46986710 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr1:46985789-46985800 | CTTCTGGGAAA | + | 6.62 |
|
| | 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 |
| GH01I046519 | chr1 | 46985499 | 46989059 |
|
Enhancer Sequence | TACAGGCGTG AGCCACCGCC TGGCTGAGCC ATGGCGCCCG GTAGTTCCCC CTTCTCTTAG 60
GCCTTGGCCA ATGTTCTTGC AGCTCAGGGG TCTGGTTCCT TAGGGGCCCT CAGGGAAGGG 120
GCCCCTGCTG AGAGGGTCTG GGGAATGGAC CCCTTTAGGG CTGGGCACTT CCCTCATCTC 180
TTTCCCACAG AGCTGCTCTG GGCTGGAGCC CTCCACCCCC ATCACTCATT CTCCTTTAGC 240
TTCTGGGAAA GCCGATTAGG AGGTGGCCTT CTACCCGCCC CCCTGACAAG TGTGTCTGAA 300
CTTCCAACAA AGGCCCTCAG AGGGTTGCAG AGGGAGGGCT CAGCACTGGG AACCTGACAC 360
CACTGGCCAG GGATCACCCC AGCAGCCTAG GAGGCAGCTC TGTGGGGCTG CCCACCCCAC 420
GGCAGGCAGG AATGTCGCTC TGAGAGGGGA CCTGGTCCCA CAAAGGCCTG GGGGCTGGGC 480
TGAGGCAGGC TGGAGAGGTC TTCACCTGGG AGGCCTCACA ATAAGGAAGA CAGCAAGGGC 540
CAGCACCCAG GAAGGCACGT GGGAATAGGC ATACACGCCC CCACACACTG ACAGCCTCTC 600
ACACACATTC CCCATACATT CACAGCACAC ACGCACACAC GCATCCTCTC ACACCCCTGG 660
GACATGTTGA CTTCTGCACT GGACCACACA ATCCCAGGGT GTCTGTCTCC CTGTCTCTCA 720
TGCCTGTGTA CACAGCCCCA CTGCAAACCG GCAGACACAC AGCCACGCTC TGTCGCCTGA 780
TGCTCCACAC ACCCGCTCCA CCCCCAGACA TGCATTCTTC CCGGCTTGCT CACACTCCAG 840
ACAGCCCCTG AATGCTCAGT GGCACCAGCT CCCCTGTACA GACAGCCTCT CGAGCCAAAC 900
TGCTGGCCTG GTGCCCACAG AGACTTGGTG GCGGCTGCCC TGTGATTGTG GAAGATGCCA 960
CCCAAATGCC CACATAAGAG TCAGACACTG GTCCCAGCTG CCATGTGAAC ACCCATGTGC 1020
ACCAACCCAC ACATCCACCC CAAGGGGCTG CCTTGAGCCC ACCTCTTCAC AGCATGCTCC 1080
CTCCTGCAGC AGCCTCATGG GCGTGTGACC CATGCAGTCA CACAGGGCCC TGGGCTCAGA 1140
GGGCCCGCAA TGTTCTGATG 1160
|
