Tag | Content |
---|
EnhancerAtlas ID | HS133-13472 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:75830280-75831060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:75830747-75830758 | AGTGACTCATC | + | 6.02 | GATA2 | MA0036.3 | chr17:75830838-75830849 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr17:75830838-75830849 | ACAGATAAGAA | - | 6.62 | JUND | MA0491.1 | chr17:75830747-75830758 | AGTGACTCATC | + | 6.32 |
|
| 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 |
GH17I077834 | chr17 | 75830260 | 75831390 |
|
Enhancer Sequence | ATAGAGTCTG GGATCTAGCA TGTTCTGCTT TCTGTTGCAC TTTGGGGATC AGTCTAATGC 60 CCCAGGGATG CAATAGTGCT CCTGACTCTG AAGTCAAAGG ACCTTTTGCT GCCTGTCACT 120 CAACCATAAC TGGAGCTGAC TGGGCTGATC TGTCCAGACA GCGCTCCCAA CCTCCCTCCC 180 TGGGTGACCT CCAAAGCTGC ACCCTGTTCT CAGGAGGCAT CTTCCCCGGC CAGAATCTCC 240 ATGCAAACCC CAAGGTTCTG TTGGAGGATA CTGCAGGGTG GTCACGCCTC TGAGATGACT 300 CTGCGGACCC TCCCAGCCCT GAGATCCCAC GAGGCTTTCC TACCTAGGCC TCTGGAATGC 360 CAGGAAAGGA AAGCCAAATG CTCAGGGCTC CTCACGCTCG CCCCAGTCCC TGGCAGAAGG 420 GAAGCTGCCC TAAGTCTCGC TGGCTGCGGC AGTCCTCCTG GCTGCTGAGT GACTCATCAG 480 CCTCAGCAGA GCCTACTGTG ACTGGCGTAG CTCCTCCCAC GCTTGCCCTG ACCACCCCAC 540 TGGGAGAAGG TTCTCAGAAC AGATAAGAAC TAAGTAGCAG TTACTCTTGG CCTCTCTAAG 600 GCAGGGGGAC AAAACGGACC AGGCTGACCA GAGGCAAAAC CATGGAGCAG GTGAAGGATG 660 GTCCCAGACC CCTCTCTTCT GCCAGCTCCT CCCACCCTCT TGCCATCCAA AGCAACCCCA 720 TTCCCAAGTG GGGGAGCCTC TTTGAGCTCC TTACCCCAAT CAGCCCTTCC TCCTACAGGG 780
|