Tag | Content |
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EnhancerAtlas ID | HS182-20470 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:514170-515040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr8:514244-514259 | TGCAGAGTCACCCTG | - | 6.1 | PPARG | MA0066.1 | chr8:514695-514715 | AGGGGGTGGCAGTGACCCAC | - | 6.33 |
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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 |
GH08I000564 | chr8 | 514024 | 515846 |
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Enhancer Sequence | AAGATCTTAC AATAGTGTCT GGCTATAGGA GGTGCTTACC AAGCCTTTTC TATGGTTATT 60 GATCTCTAGG GACTTGCAGA GTCACCCTGA GAGGCACGGC CATGCCTAGA CTGGAAAACT 120 GGTTTTGAAC CACAGGGCCA GGAGGAGAGA GACCGGCGGC AGGCCCTGCA GGCTGGGCGG 180 GCGCAGAGCT ACGGGCAGGG GCCTCTCTCC TCCCCAGCCC AGAGCTGTTT CTCCTTCCAC 240 CACTCAGAGC TGGCCAGGCC AAAGCAGCCT GAGCTCAGGG CCATCCACGC ACTACCCACA 300 ATACACGCTA TGCACACGCA TGCCACACAC GACACACACA ACACACCCCG TATACACACA 360 TGCCACACAC ACGCTCCATA CACAACACAT AACACAGGCA CACATACTCT ACACACACCA 420 CACACCGACA ATACCGGCGG GATGCAAGCC CGCCTCCCTC CCTGTGTTCC AGTCCGTGCC 480 AGGGACCTCG GCCTGACCTC CTGCAGGGAA AGGAAGTGGA GGAGAAGGGG GTGGCAGTGA 540 CCCACAGCTA GGTGCCCCTC CACCACGGAG TTTGTCATTT TTGTAAAGAT GTCAACACAG 600 AACATTTTTA AAGCAGAGAC GCAGCAGGAC GCGCAACTGC AGTCTCAGGC CGACCTTCCT 660 GCTTTCTCGG TGGCAAATTC CAAACCCCAG AGGAGTAAAG CCAGACCCAG GGTCAGGAAG 720 TTGGACGCCG CCCTCGCCGC TCCAGGGTTT GCCCAGAAAA GCTCTGGGTG AAACAATGTG 780 AGGAAGCTCA GGTATCGGTC AACAATGGCC TGGTCATTCC CAGCCCTTTT CAGGTTTTCT 840 GCTCCCTGGC TGAGGCCGCT GGCATCTGCT 870
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