Tag | Content |
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EnhancerAtlas ID | HS176-23950 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr20:33861060-33862070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr20:33861925-33861940 | CCATGACTCAGCCAA | + | 6.11 |
| | 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 |
GH20I035273 | chr20 | 33861341 | 33861510 |
| Enhancer Sequence | TGGTGACATG TGCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCCAGAGG ATTGCTTAAG 60 ACCAGGAGTT TGAGGCTGCA GTGAGTTACA ACTGCACCAC TGTACTCCAG CCTAGGCAAT 120 GGAGTGAGAC CTTGTCTTAA AAAAAAAAAA AAAGGAAATA AATGCTGGGA GAGAGCAACG 180 AGCTAGAGGG GGCCGTGTTA GAGATGGCTG GGAAGGAGTC TCTGAGGAGG CTTCACTGCT 240 GAGAAAGCCA ATGGCCACAG CTGCTATTTG TTGGCTGTCT TGTATACCTG ATGCTTTACG 300 CACAAGATCT CCCTTTTTGG GGAGCCTCAG AGACAGGTGA CATCAAGGAC CGAGACCAAT 360 GAAAGCCCTA GCCACGGTGG GAAGCCAGCC AATGAGGACG GCCTAAGCAA GCTGCTTTGC 420 CCACTGGCTG GGCCGCTCAG GCTGTTGCTC GAGCCCTGGG GTGGTTGCCC AGGGAGTGAT 480 TGGCAGGGCT GCCCAGCCTC TCTCCCAGAA GGCTCCCAAA GGTCCTGCAT CTGTGTTGTG 540 AAGTGATGTG TGCCAAGCCA AAAAAATCCA TAATTGCAGA GAGGTCTTGC TGTCAACACA 600 AGGTGAAATC TTGCTCCCTG CCTCCCTTGG CTCAAGCAGG AGCCAGGCTG AGGCTTAATG 660 GAGCCCACAT GAGCGGGGCA AGGGGGACCT GTGCGCACAG TGTGACAGAG CTGTGACCCA 720 GGCTTGCGTG CAAGGGGTCC TGTCTGGGCA GCACAAAGTG AACCATGTCC CAGTTCTCCC 780 TGAAGCCCCT CTGGTTTCCT AGCACCCGTA GGATGACAGG CGGACCACTC CAGGTCCCGG 840 GTGCCCCCCT CTGCAGCTTC TTACTCCATG ACTCAGCCAA GCACTGCACC CCAAACCTCC 900 AGGTGTGCCC ACCTTGCCTC CCTTGCCACA GTGCCTGTGC CCTCCTTTTC ACACTGCCCC 960 AGAGCAGGTG CCGGAAGTGT CTGGGAGTGG TGATGCTGGG CTGTATTTCT 1010
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