Tag | Content |
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EnhancerAtlas ID | HS055-08811 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr9:117038050-117040480 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:117038888-117038900 | AAACAAACAAAC | - | 6.32 | GFI1 | MA0038.2 | chr9:117040276-117040288 | CAAATCACTGCC | + | 6.04 | HSF1 | MA0486.2 | chr9:117039169-117039182 | TTCTCGAAGGTTC | + | 6.23 | MEF2C | MA0497.1 | chr9:117039829-117039844 | TTCCTAAAAATAGCA | + | 6.25 | RREB1 | MA0073.1 | chr9:117040437-117040457 | GGTGAGTGGATGGTGTGGGT | - | 6.08 | TP53 | MA0106.3 | chr9:117039141-117039159 | AACATGTACAGACAAGTT | - | 6.41 | TP53 | MA0106.3 | chr9:117039141-117039159 | AACATGTACAGACAAGTT | + | 6.59 |
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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 |
GH09I114276 | chr9 | 117038448 | 117042260 |
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Enhancer Sequence | GAGTGTGCAG GCCCCTTGCA GCGCCTGGAG CTCTGGGGTA CCCTGAACTC TCATGCCTGT 60 GCAGGCGGCT GGGCGGGAGG GCTTTTGGTC GTGCCACTGA AGGATCTTCT GCTGTGGTCC 120 TTTCTCCACC TGGCAGTTTG CCAGAGAACC AATCTGCTCA ATGCTCCATG GCTCTGGAGA 180 ACAACCTCGG TTACTCATCC TCCTGGCTGC CCTGCCCTGT GCAAACCTGG TCCCTGCCGA 240 CCTCATCTCA TCCATCCCCC ATATCCAGAC ACACTAAACT TTTTTCAGTT TCTTGGACAA 300 GCTGTGGCCC TTACCCCTGG GCCTTTGCAT GTGCTCTGTC TAGGACACTC TCCCTTCTTC 360 ACTCCCCTGT CACCTGCTTA AGTTCTATTT GGCCTTCAGG TATCACCATA GACATCACCT 420 GCTCCAAAAA GCCATTCCTG CCCCCAGGCT GGGCCATGAG CCCTCAGGGA CATGCATAAC 480 CTTCAGTGTA TGTCTTGGCT CCATGAAGAC CAAGACCTTT TCTGGCCTTC ATTTACGTCT 540 TTAACAGTGC CTTGGCCAGG TGCGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGCAGC 600 CAAGGCGGGT GGATCACTTG AGGTCAGGAG TTGGAGACCA GCCTGGCCAA CATGGTGAAA 660 CCCCGTCTCT ACTAAAAATG TAAAATTAGT CAGGCATGGT GGCGCATGCC TATAGTCTCA 720 GTTACTCAGG AGGCTGAGGC AGGAGAATCA CTTGAACCTG GGAGGCGGGG GTTGCAATGA 780 GCTGAGATTG CGCCACTGCA CTCCAGCCTG GGCAACAGAA CAAGACTTTG TCACAAAAAA 840 ACAAACAAAC AACAACAACA ACAAAACCAG TACCTGACAC ATAAGAGGTG ACCAAAGTCT 900 GTTTGTTGAT TGAGAAGACG GAGGAACTCT GCTCTTCCAC CCTAACAGAA ATGTACTTAG 960 TCAGTCCACA GACCCTCACG AGCATCTTCC CTGGGCCAGG TCCCCTGAGA TTGAAGAGGT 1020 AAATCAGAAA GCATCCCTGA CTTTGAGGGA CATAGAAGCC AGTAGGGAAG GGAGCAGAAT 1080 TCTCCTGTTT CAACATGTAC AGACAAGTTG CCCAATGCTT TCTCGAAGGT TCCCTCTTTG 1140 ATACCGATAG CAACCCCTGA GGATTGGGAA AATCGGAGAG GTAAAGGAAA CTTCCCAGGC 1200 TCACACAGTG AGAAATGACA AAGCTGGAAT TTGAACTTAG GCCTGCATGA CTCTACGCAT 1260 ACTGCCCCTG TGCTCTGGCA GAGTTGGAAT CCAGGGCTTG GCTGTGGGGC TGTGAGGATG 1320 AGCTGGAGGC AGGTGGAAGC TTGATTTTTG AGTGTCGCAA ATACTGGACT GATGACTCGG 1380 AACTTGACTT GGTAGTGGGG GGCAGTGGTA GTCTTGTACA GTTGAGCAGG GTTTGTGTGA 1440 CCCAGGAGTG CTGGGTCGGT TCAGTTGAAC TCCTTGGGAC CCGTGGATTA GGTGGCCTCG 1500 TAGACAAAAT GCCCAAATGC ACAGGCCTGC TGGCATCTAC CTTGAGCCAA CCAGGTGGTG 1560 AGAACTCATG CCTCTGCTGC CATCCCAGTC TCCCTGGGGT GTCATTTTCA CTCTTCATCC 1620 CTCAAGCGGA GAGACTGACG TTGTTACCTA GGCAAAGCAG CCCAGTTTGA TTCAGGCCTG 1680 CTCTTGACAC TGTTTTTCCC CCCTGAAGTG TTTACATGAC TAACCTAGGA CAGATCCAAG 1740 TTAGCCTGCA ACAAACTATG GTTGTGGGAA AATATTTGTT TCCTAAAAAT AGCACTGAAG 1800 TGCCAATCCC CCTAAACAGC TGCAACAGAA TGAACTCACC AAACTAGAGA AGAATACGAG 1860 GGCGCTGAGT CAGCCAGGAG GCTTCCCCCA GGCTTGACTC AGTGGCGGGC TTGACTCAGC 1920 GGCGGGGAAG TAGGCCAAGG GGAATTTAGC AGGAGGGTCC CGGGCCAGGA TTCTGCATTA 1980 GGAACTTGGT CTGCGACCTT TCACCCGCCC CCTGCCCTCT CTGGTTTTGC CCTTGGAGGG 2040 TTTGGAAGGA ATGTGTGCTA AGATTACTTT GAGCTCCAGC GTTCTAGGGA CCCTTTTTTA 2100 GTGAGTGTTG AGTATCATGG CTGTGGAATG GGCAGGAACA CATGGCAGAA ATAGCCTTGG 2160 AACCAGAGTC CTGAGGTTGA ACTTGAGTTT CTGGCTCTAG TAACCCATTC TCTGTGTGAC 2220 TTTGGGCAAA TCACTGCCCC TCTCTGAGCC TTGGTTTTCT TATCTATAAA GAATAAATAA 2280 AACTTAGGGT AGGAAAGCAC TTTATAAAAT GCACCAGAAA TATAGAAGAT TGTCTTTATA 2340 AATTTAGAGG AGAAAGTGAC TAGAGGCTGG TGGTGGCTGG TGGTGATGGT GAGTGGATGG 2400 TGTGGGTGGG GGCAGCAGCA ATGGTAGTGG 2430
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