Tag | Content |
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EnhancerAtlas ID | HS176-41478 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:33211360-33212420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr9:33212257-33212278 | GGAGCAGCAGAAGAAGGGAGG | + | 6.48 | ZNF263 | MA0528.1 | chr9:33212273-33212294 | GGAGGAGGAAAAGCAGGAAAA | + | 7.86 |
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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 |
GH09I033211 | chr9 | 33211358 | 33212634 |
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Enhancer Sequence | CAGGTTCAAA CGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGCATGCACC 60 ACCATGCCCA GCTAATTTTT ATATTTTCAG TAGAGACAGG GTTTCACCAT GTTGGCCGAC 120 TGGTCACGAA CTCCTGACCT CAAGTGATCC GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT 180 TATAGGCGTG AGCAACCATG CCTGGCCTAT ATGTTTCTTT TATTTCACCT CACCTTCACT 240 GTGACATTTA TGGCCTAATT TTATGAAATC ATGATGTAGT TTGGTTATAT TATCTACGTA 300 TGCTAAAGGT GGTGTTGTAA AGTATTTATT ATAAGAAAGG GGCACTGGAT CACATAACAC 360 TGAGAACTAC AGGTGTAGGT GACTCATAGC TCCACCTAGA GCAAGCACTA AGTGTTCACT 420 GCATAGTATC TATTTTTATT AAGGGTGTTA TCACCCTTCT TCACTTCCAG GCACAATCAG 480 GTTTAGATCT TGGAGATCAG TCGTGTTGTG AGTCACCAGA GAGGAGCAGG CACAGCTTGG 540 AGCCTGTTCC CCTGGGGAGG GTGGCACTGA GTGATGCAAG CCTGGGTCCC AAGAAACCCT 600 GGCCCTGATG CTGCTGCCCC CTCTCTGGGA GCAGGAAGTC TCCAGGGGAA AGGACTATTT 660 CTCTAGAGCC CTGGAAATCC CAGATTAACC CTCCTACTAG GTAGATCTAC AGTGTTCCCT 720 CTGAGCATAC CAGCATCTCA AGTTTCCCAC TAAAGCAGGG GGCTGGGCCA GGCTTGGCTC 780 CAGAGCTGCG AACAGCCTGG ACAGAGCTGA CATCAGCAGT TAGGCCAGGT TGGGGAAGGG 840 TAGGGTTAGC CCCCAGCAGC TGGGCTGTCT CACCCATAGG GGAGGAGAGA AGAAGAGGGA 900 GCAGCAGAAG AAGGGAGGAG GAAAAGCAGG AAAAGGAAAG TGAGCCCAGG GAAGTTTGCT 960 CAGGACAGGC TTTTGCTGTA GGGTGGAGGA ATTTCTCTAG CGGTAGTGTA CCACTACACT 1020 TCAGCCTGGG AGCAGGATTC CTCCAGCTGT AAAGTGGAGT 1060
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