Tag | Content |
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EnhancerAtlas ID | HS098-37378 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:46525100-46526060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr22:46525372-46525393 | GGAGGAGGAGGAGGAAGAGGA | + | 10.86 | ZNF263 | MA0528.1 | chr22:46525369-46525390 | GCAGGAGGAGGAGGAGGAAGA | + | 6.77 | ZNF263 | MA0528.1 | chr22:46525378-46525399 | GGAGGAGGAAGAGGAAGTGGC | + | 7.36 | ZNF263 | MA0528.1 | chr22:46525375-46525396 | GGAGGAGGAGGAAGAGGAAGT | + | 8.7 |
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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 |
GH22I046129 | chr22 | 46524881 | 46527592 |
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Enhancer Sequence | GAACAGAATA GTCAGTGGAG AGGGGAAGGA GATGGGGAAA CTGAGGCACA GGGAGTGAAG 60 TGCCCAGTCC AGGCCAGCAC GGCCTCAGGT TCCACGCGGC TGCTTTCATC CCTGACACTC 120 GCTCGTCCAC CCCAAGCCTG TGCCAGCCCC CAGTGTCTTC ACCCAGAGCC TGTGCGGCTG 180 GAGGGGCTCT CAGCCCAGGC AAGGGCTGGC GGCCAGCCAC CCGAGGTGAC CTGCAGCTGC 240 AGAGGGGTGG CCTTGGTGCC TCTCTTGCTG CAGGAGGAGG AGGAGGAAGA GGAAGTGGCC 300 CCTCTGCTTT ACGGGGCTGT GATTCCAGTG GTAAATGCGG AAATACGGCT TGGCTGAGTG 360 CCGCGTTCGG CCAGGGCCAG CTCCCAGGAA CAGCCGGGCT GCGAGGCCAT GACCCAGGGC 420 CTGGGAACAC AGTGAGGCCT GGCCATGCTG CGAGGCCTCA GAGGGGCGGA CTGCTTAGGA 480 GGCCAACGAC CTTCCTAAGG GTGGGCAGTC AGGGAAGGGC CAACAGCATG CCCGCTGTGT 540 CCTCAGGCGG GCCCTCCCTC CCTGGGACCC TCCCAGTGCC AGCCTCCTGC CTGGGCCAGG 600 CTGGGAGCTC CCTGACTGCT CTGGTCCCTG GGCTGCTCCC ACGAGCCTGA CTCTGACGGT 660 GTCTGCTGCA CATCATCCGC GGAGTCCCGA GTTTCGGCCA CTGCGGTCGT CCCCATTTCA 720 CAGCCAGGAA ACAGAGGACA GGGGAAGTCA ACTGGAGGTC ACGCGGTGGT GAGTGACAGA 780 GTGGGTGTTG CAGGCAACCA CTGGACAGAG CCACAACCAC ACTCTCCCCA GCACACCCCA 840 CTGCCCCTGT GCTGGGGGAC TGCTCCCCAT TTCACAGATG GGGAAACCAA GGCTGGCGGG 900 AGGAGCAGCA GGAGCACATC CGTGGACTCT AAGTCAGCAC CCTGCCTGCA CACGCAGCCC 960
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