Tag | Content |
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EnhancerAtlas ID | HS133-18713 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:25117240-25117810 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr20:25117514-25117525 | CATGAGTCACC | - | 6.62 | FOSL2 | MA0478.1 | chr20:25117515-25117526 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr20:25117515-25117526 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr20:25117514-25117525 | CATGAGTCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I025136 | chr20 | 25116932 | 25117871 |
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Enhancer Sequence | ACCATGAGCC AATAAATTTC TGTTCATTAT AAATTGCCCA GTCTATGGAA TTCTGTTATA 60 GCAGCACAAA GCAGACTAAC AGGGCTGCAG TCAGATGTCA GCCTGGGCTG CATCATTTGA 120 AGGCTCTGCT GTGGCCAGGG GATCCACTGC CAAGGCAGCC CTCACTGGCT GCCGAGCTGG 180 TGCTGGCTGC TGGCAGGAGG CCTTAGCATC TCTCTGTGTG GGCCTCCCCA GGGCTGCTTG 240 GGCGTCCTTT TGGCATGTGG CTGGCTTCCC CCAGCATGAG TCACCCAAGA GAGCAAGGCG 300 GGAGCTGTAG TGCCTTTTCT GACCCATCAA CATTCTGCTG GACACAGAGG CCAGCCCTGA 360 TTGAATGTGG AAAGGACTGC ATGAGAGTGT GGCTCGAGGA GGCCAGAACC ATTGGCAGCC 420 ACCTGGGAGA CTTGGCGATC ACAGAGAGAG GGAGACAAGA CATTGTATGG AAACTGTGAG 480 TGGCTGTGTC AAGCTCATAA TATTCCATAA ACATGGGTGG GGAAGATAAG GATGAATGAT 540 TAGCAAGGAA AGGAGAAAAA ATAAAAAGCA 570
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