Tag | Content |
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EnhancerAtlas ID | HS101-02847 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:155282820-155283850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:155283512-155283530 | GGAAGGAAGGGAAGGAGG | + | 6.71 | EWSR1-FLI1 | MA0149.1 | chr1:155283508-155283526 | GCAAGGAAGGAAGGGAAG | + | 7.02 | ZNF263 | MA0528.1 | chr1:155283510-155283531 | AAGGAAGGAAGGGAAGGAGGA | + | 6.3 | ZNF263 | MA0528.1 | chr1:155283513-155283534 | GAAGGAAGGGAAGGAGGATGA | + | 6.67 |
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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 |
GH01I155313 | chr1 | 155283531 | 155283932 |
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Enhancer Sequence | GAAGCAGAAA TTGAAAACTG GCAGCTCACT GACAGTATTT TGAAAATGTT TTACAATTAA 60 GTCTCCTAAA TTTAACAAAG AGATTTCACA CTAAAACCTA GATTTCTAGC ATGGCTTGGG 120 AAATTGTAAG ATTTGGGTCC ATGTTCCCGC ATAGCAACAA TTGGCTGAAG CTGAGTGGAT 180 GCAACTTCTG CAAGACGGCA TGTGTTCTCC TGTGTGCTTT CTCTAGTTTG CTCCAATCCC 240 CACATCCCCT TGTCTTCTAT ACCAGTTCGT CTTGGTCTTG AAGGTGTCTA GTTTGCTGGC 300 ATGGCCTAAA GCTTTCATTA GTGGCAGGGG GACTGGGTTC TGGGAGGGGT GCCATGCCCG 360 AGGAGGGTGG CAGTGAGCCC AAAAGGGAAG AGCATTCAGA ACTTGGTGAG TGACGATGAT 420 GCTGAGTGCC TGGCCTGAGA GGAGCAGCTG GCTCAAGGGA AGACGTGCTG AGCACAGTCA 480 GCCCGGGTAC GTTCTTGGTA TGGGTGGAGC AGGTGGATCT GCCTGTCCTG TGGGCGGTGG 540 AAATTCCAGT CTGGAACTTG TCGGGGAGAT GGGTCTGGAG AATAGAGATT TGCTTCCAAG 600 GAGGTAATAG GCCCATGGCA TCCAGGGAGA GGGCCCTGGA TGACAGGGAT GCTGAGGGGC 660 TGAGGGGTTC AAAATATGGA GATGACAGGC AAGGAAGGAA GGGAAGGAGG ATGAGGGCAG 720 AGCAGAGGAG TAAAGCTATG GGGGCCAAGG GAAGCAAGAC CTTGAGGGGC CAGTGGTTAA 780 CTGGTAGAAT CAGTTCATTT TTTTTTTGAG ATGGAGTCTC TCTCTGTTGC CCAGGCTGGA 840 GTGCAGTGGC ACCATCTTGG CTCACTGCAA CCTCTGCCTC CCAGGTTCAA GCAATTCTCC 900 TGCCTCAGTC TCCTAAGTAG CTGGGATTAT AGGCACATGC CACCATCCCT GGCTAATTTT 960 TGTATTTTTA GTAGAGACGG GGTTTCACCA TATTGGTCAG GCTGGTCTGG AACTCCTGAC 1020 CTTGTGATCC 1030
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