Tag | Content |
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EnhancerAtlas ID | HS105-42446 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:29265090-29265980 |
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 | GCATAGTGCT CTGGGGTTCA TAAACCAGCC CAGGCACACT GTGTCTTGTT TTGACATTGC 60 CCTGCAGCTA CAAGCATTTA TTCAGCACCT GCAGTGTGCT GTGCACCGTG GGAGCATGGT 120 CTGGCACAGG TCTCTGCTGG ATATGCATTT TTAAGTGTTC CCCAAATTCA CTTCTTTCTG 180 GCTCTGGGGA GAGGGGATGT TTGGGGCCAG AGGCGGGAGC CCCTGCTGTG TCTAGATGTC 240 AGGTCTAGAT GTGTCTAGGG TCAGGTTCCA GCTCATGCTG AGGTCTGAAG GGAGTGGGTG 300 GATGAGCAGA AAGAACACTC GGGGGGGCTA CAGGCAGGTG AAAGATGATT TTATTCAGCA 360 GCAGCTCTCT GCAGCAGCTT ACTCTCACAC CATCTGCCCT GTCTCAGCTG CTTAGTCTGT 420 TGGCTCCCAC ACACAGCTGC GCCGGCTCTC CCTTGCCTTC AGGGTCAGCA GCTTAACTCT 480 TTCCCTCTGG GCACAAGCCG TTTCCTAGCT CCGTGTCCGA CTGCCAGACG GGCATTCTCT 540 CTTACAGGGG GCAGTAGCTT CACTCTCTCT CTGGGCACAC ACAAGCCTGC ACAGTGTCAG 600 CAGGGCAATT ATGCCTTTTA CAGACCATAG TGGCACAGGG CCAAGGCATG GCCTTCCCAT 660 GTTACGACTG TGATAACAAG TGGAGTTATA CGTCTGTGCT CTAAACTTGC TGAGTCACTC 720 TGGATGTTTA CCTTGGCCTA TCCTTGACCA AAGCACAGCC ATGTTCCTTA CATTAGAGAA 780 TGTTCTAGGC TGAGCATTGT GGGAGGTGAC GGAGGAAGAA GTCCTTGTCT TCAAATCTGA 840 GCCCAGGTAA ATGATGGGGT GGGACAAATA GAAACACCTG GAAACAAACA 890
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