Tag | Content |
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EnhancerAtlas ID | HS101-04881 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr10:26650170-26651920 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:26651800-26651821 | GAGGGAGAAAGGGAAGAGAGG | + | 6.16 | ZNF263 | MA0528.1 | chr10:26651793-26651814 | GGAAGAGGAGGGAGAAAGGGA | + | 6.65 | ZNF263 | MA0528.1 | chr10:26651796-26651817 | AGAGGAGGGAGAAAGGGAAGA | + | 7.68 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATTCTTAGA TGTACAGGGA AATGATTCTG TAGTTTTTGC ACCAAATTTT GCCAGTCAAG 60 AGAAATGACC TTATAAAGAA ATTCAAGAAG CAGAGAGTAG CTGTGACCCT CCCTTCCACT 120 AAGGTGGTAC CAGCTTTTCA GAGGGAGGAA TGTTTCAGCC TCATAACTAC CTGCCACTGA 180 AAATGTGCTT AGACTGTTCC ACATTATTTC CATTTCTAGG TAAAATCCAG TGTGGAAAGA 240 ATTTACAGCA TCATAGGCAG ACGTGATAAT CAAAATATTT AGTGTCTGGT AGGGTGGGGA 300 TATGGGCTGC TCAGAATGGT AGTAGCCTAA CCAGTCAGAC CAGATGCCAT AGTACGTACC 360 TGTCAGTATC AGCTCTGGTT TTGGAAATCT ATGGAACAAT GAATCCAAGA GACTAAGGGT 420 ATCAATATTT TGTATTGCAT GCATTTTCAG TATGTCTTTT GCTCATTTGA AAGAAAGAGA 480 TGGTTTGGGT AAGCGGGAAT TTGGAAAGCC TCATTTCTTA AGGTAAAACT GAGTTGTACA 540 TTATATCATC ATGTAGTTTC CTCCTAAGTT GAAGGTGCTG GACACGGTGC CTGAATAGCA 600 CAGGCATAAT AAGTAGTTAA AATAGTGCTG TTTGTATTGT ATCTTTTCTT GTCAACAAAT 660 GCTTATCCAG AATTTATTGA AAATCTGTGA CCACCCTGAG GACCTGGCTG GGTAATTTAG 720 AGGCTCCACA GCAATATCTG ACTATACAAA AAAAAATCAG TTGAGTGCTC ACAGAAAATG 780 ATAACAAGGA AGAGGAAATT GATGACTGTA TAAAGTGGAC CATACCAGCA GATAGGAGAC 840 AAAGAAAAGA AAGTCAACAT AGAAATGCCA AAATAGAAGA GGAAGTAAAA AGGGAGCTGG 900 GAAAACGAGG TATTCTAAAA ATAGGCCTTG TGAAATTGAA TAGCACTAGG ATGGGAAGTA 960 GCCAAGTTTG GGCACATGAA GCTAAGAACT ACAGTGACTT ACATGGTAGA AAGCTATGCT 1020 CAGAAAACTT TTCCTTGTCT TCTCTTGTCA CTCAGGACAA AAGGAGTCTT TTTTGTTTTT 1080 ATTTTTATTT ATTTTTTAAT TTTTTGAGAC AGAGTCTTGC TCTGTCACCC AGGCAGGGGT 1140 GCAGTGGCAT GATCTTGGCT CACTGCAACC TCCGTCTCCT GAGTTCAAGC CATTCTCCTG 1200 CCTCAGCCTC CCCAGTAGCT GGGATTACAG GTGCGCACCA CCATGCCCAG CTAATTTTTG 1260 TATTTTTAGT AGAGACAGGG TTTCACCATG TTGGCCAGGT TGGTCTAGAA CTCCTGACCT 1320 CATGATCAGC CCACCTCGGC CTCCCAAAGT GCTGAGATTA CAGACATGAG CCACCACGCC 1380 TGGCCAAAAG GAGTCTTTTA AAAAGCCAAC TGAGCAAGGC CTCCAGGACC CTTAGGTAGG 1440 CTCAACAAAT GTACGGATCT TGAAGCCTTT TCTCCACTAC TCACACCCAC ACTCTAGCCC 1500 TGGGATTTAG TTAGTGCTGG AAGTCTGTGA TCCTTTGTTA GCATTAGATC ATGAATAATA 1560 AAGTGACAAG AGACAGCATT TAGAAATAAC TGCAGCTACC AAGAAAGAAA GTTTTGCCCT 1620 GTGGGAAGAG GAGGGAGAAA GGGAAGAGAG GAGGAATGAG CCTCTTGTAA CCACAGTGCC 1680 ATGCTATGCT TACAGCAGAG GAGGTTTTCT AACGAAGACG TTCGGTCAAC TTGGATACAT 1740 AAATGTTGAA 1750
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