Tag | Content |
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EnhancerAtlas ID | HS082-17835 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr2:29265210-29266140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:29265795-29265810 | CTTGCTGAGTCACTC | - | 6.48 | Nfe2l2 | MA0150.2 | chr2:29265797-29265812 | TGCTGAGTCACTCTG | - | 7.73 |
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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 |
GH02I029042 | chr2 | 29265121 | 29266003 |
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Enhancer Sequence | CTGGCACAGG TCTCTGCTGG ATATGCATTT TTAAGTGTTC CCCAAATTCA CTTCTTTCTG 60 GCTCTGGGGA GAGGGGATGT TTGGGGCCAG AGGCGGGAGC CCCTGCTGTG TCTAGATGTC 120 AGGTCTAGAT GTGTCTAGGG TCAGGTTCCA GCTCATGCTG AGGTCTGAAG GGAGTGGGTG 180 GATGAGCAGA AAGAACACTC GGGGGGGCTA CAGGCAGGTG AAAGATGATT TTATTCAGCA 240 GCAGCTCTCT GCAGCAGCTT ACTCTCACAC CATCTGCCCT GTCTCAGCTG CTTAGTCTGT 300 TGGCTCCCAC ACACAGCTGC GCCGGCTCTC CCTTGCCTTC AGGGTCAGCA GCTTAACTCT 360 TTCCCTCTGG GCACAAGCCG TTTCCTAGCT CCGTGTCCGA CTGCCAGACG GGCATTCTCT 420 CTTACAGGGG GCAGTAGCTT CACTCTCTCT CTGGGCACAC ACAAGCCTGC ACAGTGTCAG 480 CAGGGCAATT ATGCCTTTTA CAGACCATAG TGGCACAGGG CCAAGGCATG GCCTTCCCAT 540 GTTACGACTG TGATAACAAG TGGAGTTATA CGTCTGTGCT CTAAACTTGC TGAGTCACTC 600 TGGATGTTTA CCTTGGCCTA TCCTTGACCA AAGCACAGCC ATGTTCCTTA CATTAGAGAA 660 TGTTCTAGGC TGAGCATTGT GGGAGGTGAC GGAGGAAGAA GTCCTTGTCT TCAAATCTGA 720 GCCCAGGTAA ATGATGGGGT GGGACAAATA GAAACACCTG GAAACAAACA GGTGCCATTC 780 ATATGAAAAT CTATTCTTAA CGCAATTGAC AGCTTTACCA ATGCACCCCG AGACCTTATC 840 TTGCTAATTA CTATATTCTA GAAGCTGGCA TCTCATTTAT CTCCCAGGGC AAATTATTTT 900 AAAGCCGCTT GATTTGCGGA TGGAGCTTTT 930
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