Tag | Content |
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EnhancerAtlas ID | HS133-18930 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:33861200-33862070 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr20:33861925-33861940 | CCATGACTCAGCCAA | + | 6.11 |
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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 |
GH20I035273 | chr20 | 33861341 | 33861510 |
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Enhancer Sequence | AAAAAAAAAA AAAGGAAATA AATGCTGGGA GAGAGCAACG AGCTAGAGGG GGCCGTGTTA 60 GAGATGGCTG GGAAGGAGTC TCTGAGGAGG CTTCACTGCT GAGAAAGCCA ATGGCCACAG 120 CTGCTATTTG TTGGCTGTCT TGTATACCTG ATGCTTTACG CACAAGATCT CCCTTTTTGG 180 GGAGCCTCAG AGACAGGTGA CATCAAGGAC CGAGACCAAT GAAAGCCCTA GCCACGGTGG 240 GAAGCCAGCC AATGAGGACG GCCTAAGCAA GCTGCTTTGC CCACTGGCTG GGCCGCTCAG 300 GCTGTTGCTC GAGCCCTGGG GTGGTTGCCC AGGGAGTGAT TGGCAGGGCT GCCCAGCCTC 360 TCTCCCAGAA GGCTCCCAAA GGTCCTGCAT CTGTGTTGTG AAGTGATGTG TGCCAAGCCA 420 AAAAAATCCA TAATTGCAGA GAGGTCTTGC TGTCAACACA AGGTGAAATC TTGCTCCCTG 480 CCTCCCTTGG CTCAAGCAGG AGCCAGGCTG AGGCTTAATG GAGCCCACAT GAGCGGGGCA 540 AGGGGGACCT GTGCGCACAG TGTGACAGAG CTGTGACCCA GGCTTGCGTG CAAGGGGTCC 600 TGTCTGGGCA GCACAAAGTG AACCATGTCC CAGTTCTCCC TGAAGCCCCT CTGGTTTCCT 660 AGCACCCGTA GGATGACAGG CGGACCACTC CAGGTCCCGG GTGCCCCCCT CTGCAGCTTC 720 TTACTCCATG ACTCAGCCAA GCACTGCACC CCAAACCTCC AGGTGTGCCC ACCTTGCCTC 780 CCTTGCCACA GTGCCTGTGC CCTCCTTTTC ACACTGCCCC AGAGCAGGTG CCGGAAGTGT 840 CTGGGAGTGG TGATGCTGGG CTGTATTTCT 870
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