Tag | Content |
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EnhancerAtlas ID | HS187-23572 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:21998210-21998960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr8:21998379-21998390 | TGCTGTTTACA | + | 6.14 | PPARG | MA0066.1 | chr8:21998235-21998255 | GAGGGGCACCATGCCCCACT | + | 6.18 |
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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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Enhancer Sequence | CTGGAAGAGC AGCCATGGGG AGTGTGAGGG GCACCATGCC CCACTCCCAC CTTGCCAAGT 60 GGCCATTTCC CCCCACTGGG GTGCAAGGTG GCAGTACCCG CCCTGTTTTT CTCGCTTGGC 120 TTGTACAACC CGTGCCTGAG TCAGAGCCCT GGAGGCCACC TCCCCACCCT GCTGTTTACA 180 AACATCCCAA GCCTGCCCAG GCCTGCACCG GTGGCCCATG GGTGCATGAT GGAGTGAGAG 240 GACAGCCACT CCACGAAGTG GGTGAGAACA CCAGACTGTC CCCTCCCATG GGCATGCAAT 300 CAGGCCCAGG GTCACCAGAC CTGACACTGC TGGGTTGCAG ATAGGGCTAT GTGAGCCAGA 360 TGTTGGCATA CTCAAAGGTG AGGAATAGGA TGGTGAGTCA TGTGACTGCT CAGATGGCAA 420 GCAGGCACCT GGATTCTCCG CCCACAACGT GCCATATCAC CTTGTGTTTG CCAAGGGGCA 480 GCAAGGTAGG CCTGTGGCCC TCGGCTCCAC GCATCTGTTT GCAGTGTGTG TGGCGTGCGG 540 CAGGGGTCGT TCTCAGCCAA CGAGGCTTGG TGGGGCGGGT AGCCTGCGGT GCCCCAGACA 600 CCGCGTGCAA GCCCACAGGT CCGTTAACCC TTGCATGGAG TGCTGGAGGG TGGAGCTCAG 660 AAAGTTCCTC CTCCCACTAG ACGTCCACAG CTTCCACCAC AGGGGCGGGA CGGCACCCCG 720 GGGTAGAGGA GGTCTGAGGG CGGCCATACT 750
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