Tag | Content |
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EnhancerAtlas ID | HS078-16481 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr9:100565390-100566850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr9:100565819-100565831 | CGTGACGTCACC | + | 6.32 | CREB1 | MA0018.3 | chr9:100565819-100565831 | CGTGACGTCACC | - | 6.32 | Crx | MA0467.1 | chr9:100566325-100566336 | GAGAGGATTAG | + | 6.02 | EGR3 | MA0732.1 | chr9:100565783-100565798 | AGCGCGGGGGCGGGG | - | 6.01 | EWSR1-FLI1 | MA0149.1 | chr9:100565483-100565501 | GAAAGGAAGAAAGGAGAG | + | 6.34 | EWSR1-FLI1 | MA0149.1 | chr9:100565479-100565497 | GGAGGAAAGGAAGAAAGG | + | 6.86 | IRF1 | MA0050.2 | chr9:100565447-100565468 | AGAAAGAAAATAAAAGAAAAA | - | 6.13 | IRF1 | MA0050.2 | chr9:100565453-100565474 | AAAATAAAAGAAAAAGAAAAA | - | 6.27 | KLF16 | MA0741.1 | chr9:100565788-100565799 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr9:100565840-100565850 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr9:100565789-100565799 | GGGGCGGGGC | - | 6.02 | ZNF263 | MA0528.1 | chr9:100565528-100565549 | AGAGAAGGAGGGAGGGAGGAA | + | 6.09 | ZNF263 | MA0528.1 | chr9:100565535-100565556 | GAGGGAGGGAGGAAGAGAAAG | + | 6.24 | ZNF263 | MA0528.1 | chr9:100565605-100565626 | GAAGGAGATGGGGAAGGGAGA | + | 6.48 | ZNF263 | MA0528.1 | chr9:100565492-100565513 | AAAGGAGAGAGAGGAGAAAGA | + | 6.52 | ZNF263 | MA0528.1 | chr9:100565516-100565537 | GAAGCAGGCGGAAGAGAAGGA | + | 6.5 | ZNF263 | MA0528.1 | chr9:100565705-100565726 | CAGGGAGGAGGAGGAGGAAGG | + | 6.75 | ZNF263 | MA0528.1 | chr9:100565539-100565560 | GAGGGAGGAAGAGAAAGGAAG | + | 6.9 | ZNF263 | MA0528.1 | chr9:100565566-100565587 | GAAGGAAGGCGGGAGGGAGGA | + | 7.01 | ZNF263 | MA0528.1 | chr9:100565476-100565497 | AGAGGAGGAAAGGAAGAAAGG | + | 7.15 | ZNF263 | MA0528.1 | chr9:100565531-100565552 | GAAGGAGGGAGGGAGGAAGAG | + | 7.48 | ZNF263 | MA0528.1 | chr9:100565708-100565729 | GGAGGAGGAGGAGGAAGGACG | + | 7.79 |
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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 |
GH09I097801 | chr9 | 100564155 | 100566516 |
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Enhancer Sequence | CGCCATTGCC CTCCAGCCTG GGCGACAGAG GGAGACTCCG TCTCAGAAAA AAAAGAAAGA 60 AAGAAAATAA AAGAAAAAGA AAAAGGAGAG GAGGAAAGGA AGAAAGGAGA GAGAGGAGAA 120 AGAAAGGAAG CAGGCGGAAG AGAAGGAGGG AGGGAGGAAG AGAAAGGAAG CAGAGAGAAG 180 GAAGGCGGGA GGGAGGAGAA AAGGAAAATT AAAAGGAAGG AGATGGGGAA GGGAGAAGGA 240 AACGGACGGA AAGAGGGAGG AATGAGAGGG ATAAAAAGGA AGAGATGGGA GATGGGAAGA 300 AAGAAAAACA GCTGACAGGG AGGAGGAGGA GGAAGGACGA AGCGGCGCAG GTGGACAGGT 360 GGCCTCGCAT CGCTTCCTCC CCAGGCCCGG CCCAGCGCGG GGGCGGGGCA ACCGCGGGGC 420 GTGGCTGCGC GTGACGTCAC CGCCCCCGCC GCCCCGCCCC GTCCCCGCTC CCGGGCCTTG 480 TGAAATCGCG CGCGCTGGCG GCCGTCGTAG ACCGTGCAGC TCTCCTTGGG TGGCTGCGAG 540 TGCCTTGGCC GTGGGCCCTG TGCGCGGCCA GCCCCGGCGG CGGGAGGGCG ATAATTGCCC 600 AGAGACGCAG CACTTACCTG GGCCGGTTGT GCAAGGCGCG CGGGGGGAGG CCCCGGGCGG 660 CGGCTCTCAC GCCTCAGCGG CCAGGCATGC GCGGGGGCGA GGGCGGGCCA GGGTCCCGGG 720 GAGCGCCTCC AGCGGTTCCC GTTGCGGACG CCGCCCCATT CTTCAGGAAA GAGCCGCCGC 780 CCGTCACCGC TGGGGATGGG GAGACCCGCG CTCCCATCCC GCTTGGCCAC CTGCTGGGGT 840 GAGTGGCGTC GGTCTAGTTC CACACGTGCC TCTGAACCCC AAGCGCCTCC TCTGTGTACT 900 AGGGGTAAAA ACGCCACCTC TCTGATCCTC TGGTTGAGAG GATTAGAAAT GATGCAGGTG 960 AGGCCTGGAA CACTGCCAGA CACACATTAG GTACATGGAA TGGTGGCCTC GATGCCCACA 1020 GACTGCCAGT CAAAACTAGG GTTAAAGTTG TGTCTCCCAC TGACTTGCTG GTGACTTTGG 1080 GATGTTTACC TCCCCTCTCT GGTCTTCAGT TTCCTCTTCA GAAATTGGAG TTTGATGCTC 1140 ACCTTCATCG TGGGCCAGGA TGATGGCCTG TGCTAGCCGT CCTTGAAAAG GCGAGGCCGG 1200 GCTGAGGGTG CACTGGGTTT AGACATAGCA AGTGTCTCCT GTCACTTGTG CCTAGTTCCT 1260 GGGGCCATGG TCCTTGGAGC TGCTGTTAGA GAGGGATGGA GTGGGACAGG GTATCCTGAC 1320 CTTACACCAG GATCCCTAGA AGTGTGATCA CACATACACA CATAGGCACA CACATATACA 1380 CATACATCAC ACTACATACA CACAGGTGCA CACACAACCC AGGGAGGTCT GACAGGAGCT 1440 GCAGTCACCC AGCACCTTCT 1460
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