Tag | Content |
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EnhancerAtlas ID | HS045-33727 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr2:29265150-29265910 |
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 | CCTGCAGCTA CAAGCATTTA TTCAGCACCT GCAGTGTGCT GTGCACCGTG GGAGCATGGT 60 CTGGCACAGG TCTCTGCTGG ATATGCATTT TTAAGTGTTC CCCAAATTCA CTTCTTTCTG 120 GCTCTGGGGA GAGGGGATGT TTGGGGCCAG AGGCGGGAGC CCCTGCTGTG TCTAGATGTC 180 AGGTCTAGAT GTGTCTAGGG TCAGGTTCCA GCTCATGCTG AGGTCTGAAG GGAGTGGGTG 240 GATGAGCAGA AAGAACACTC GGGGGGGCTA CAGGCAGGTG AAAGATGATT TTATTCAGCA 300 GCAGCTCTCT GCAGCAGCTT ACTCTCACAC CATCTGCCCT GTCTCAGCTG CTTAGTCTGT 360 TGGCTCCCAC ACACAGCTGC GCCGGCTCTC CCTTGCCTTC AGGGTCAGCA GCTTAACTCT 420 TTCCCTCTGG GCACAAGCCG TTTCCTAGCT CCGTGTCCGA CTGCCAGACG GGCATTCTCT 480 CTTACAGGGG GCAGTAGCTT CACTCTCTCT CTGGGCACAC ACAAGCCTGC ACAGTGTCAG 540 CAGGGCAATT ATGCCTTTTA CAGACCATAG TGGCACAGGG CCAAGGCATG GCCTTCCCAT 600 GTTACGACTG TGATAACAAG TGGAGTTATA CGTCTGTGCT CTAAACTTGC TGAGTCACTC 660 TGGATGTTTA CCTTGGCCTA TCCTTGACCA AAGCACAGCC ATGTTCCTTA CATTAGAGAA 720 TGTTCTAGGC TGAGCATTGT GGGAGGTGAC GGAGGAAGAA 760
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