Tag | Content |
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EnhancerAtlas ID | HS145-21258 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:131714170-131714630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PPARG | MA0066.1 | chr5:131714466-131714486 | CTGGGTCACTGTGACTCTGT | + | 6.49 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 131714394 | 131714528 | chr5 | 131714349 | 131714540 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I132377 | chr5 | 131713027 | 131714701 |
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Enhancer Sequence | CAGGTAAGGT GTCTGTCTTC TGGAGCACCA GGGGACCTCA GCACTGAGGA AGAAGCGTGT 60 GCCTGGCCCT TGATTTCAGT TGGTAGTATT CTTTCAGCGC AGGGCCCTGT ATTTTAAAGA 120 AGAGGAAGCT ATGTCTGTGA TATAGACTCC ATGCCTAGTA AGAAGAGCCA ACAAATCTGA 180 CTCCGTAATT CTTGCTAAGT AAAGAAACCT GAGCTGTCTA AGCTGAATGT ATCTGTGACC 240 CGGTTGACTA GGTAATATGC CATGATTCAC TTCTGCAGTA GCCTGGCTTG CCTCCCCTGG 300 GTCACTGTGA CTCTGTCATG CCCCTGAGCA TGGGAGAGGT TGACATCATG CACACATGCA 360 CATGTGCTAG ATTGTAGATC TGTAGTAGTG CCACGGTGTC TGCCTCTGTA GTCCCAAGAA 420 GACCAGCATT CTCTCTGCAA AGTGAAAGGA GCTCTCACCA 460
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