Tag | Content |
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EnhancerAtlas ID | HS003-29400 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr20:24745650-24747220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr20:24745828-24745849 | GAAGGAGGAATGAAGAGGAAA | + | 6.15 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAAGCCCTG GGAGGGAAAG GATGTGATTC CGGAACAAAG CTCCTGACAC CGATGGGCCT 60 CATGATGCCG AAAGGCATAA GGGAGGTGGC CGACGGCCGG GCTGTGTGTC CACAGGCTAC 120 CACCCCTCCT GCCCAGGCCA GTCTTGCCTC CTCTCCACAG ACCTTGTTGT GTAACCTGGA 180 AGGAGGAATG AAGAGGAAAA AGCTAACATT AAATTTTAAC ACAGACACAG GAGAACACAC 240 ACACACACAC ACACACATGC ACACACAAGG ACACAAGCCC ACTGCTGTTC AAATCTCAGT 300 CGCCCCAGCC TACTCCTCAT TTGGAAAAAT CACATCCATC CTTGTCTTGT GGCATGCCTT 360 CTGGGTTTGG TCATATTTAT TTGTCTGTCA CAAGTTCTTC TTGGAGGATT AGGAAGAAAC 420 CCTATGTGGA AATAATTGCA GCCAGTCAAC TGCCCCGAGA TGCCCTGAAG TTCTGTATCT 480 GCTCCCGGAG CGTTCAGTCC ATGATTCCTG CTGGGACCCT CGTCTACCTC CACACATTCT 540 GATTTTGCAG GTGTAGGGAT CTGTGCCTGC CTAGCTCCCC TGGGACTCTG CATCTGAGTC 600 CTCAAGCACC CTGGTGGGCT CGGCAGCAGC CCTGGCTTGC TGTTGGCTGT TTTCATGTTT 660 GAATCGGTCA ACACTAGCTC AGGTTGGAAA GCCCTGCATG GGAGGCCCAG CCAGTCCCAC 720 GTGGCTGGGA CTCACAGAGC ACCAACTCTG CACAAGTGCT GGGCTGGGGC TCGGGGAGAG 780 ATCCAGGCTC CACCACCGGT AGAGTGTTTT CTGCAGCCAT CTAGTCTTTG GCTGCCAACC 840 CCAGACTCTG TTGACAAGCA GAGAAGTAGG GATGTTGGAA GGGGCTCAGG AGGTTAGGAC 900 CAGGGACTGA GGGACTCGGA AGTCCAGATC ACTCTGAATG GCCCGGTGAG ACCCCACTGC 960 CTCCACCGCT GGCTGCCATT GCCATTAGTA TTCCCAGGTC TGCCAAGCTC TGCTCACAGG 1020 CCCACACCTG TGCCAGATGC TAGGTTGGGG AGATGGTGTC CCTGGCCAGC TTTGACCATT 1080 GTCAGGCTTC CCCAAAATAG AAAGGGGGCC TAGCATCAGA AAAGTGATAC ATGCCCCCTA 1140 AACACATTCT GGGGCTTGTC ACCTCGTTTC CCTGGACCTC AGATCCCCTG CATCAAACAA 1200 AAGAGGTGAG GAATCAATAG TTGCAAAGCA CAGTCAGTAA AGCAAAGGCT GGTTTAAAGA 1260 TACAAACAGG AATTGAGGAA ATATGCTTGA ATGCTCTTTT GTATGCCAAC AAACACAGCA 1320 CACAAAGCTT TTACCACCTC AGTGATCAGT TTAAGGACAG GCCCATGACC CAGCTGAAGC 1380 CACACGGGGA CAGTGAGACT TGATTCTAGG GCTTGCTTTG AGATCTCAGG GGCATACTCT 1440 CTCCTCTGGT TTGGAGGTGG CCACAAGGTG AGGCTAGAAT TGTGGGAGAC CTCCCTGTTG 1500 AGCTTGAGAA TGAACCAGCA GGGTGGAAGT GATGGAGAAA AGCCAAGTCT AAGAAGATTA 1560 AGAGTTGCCT 1570
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