Tag | Content |
---|
EnhancerAtlas ID | HS105-82743 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:117038570-117040750 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I114276 | chr9 | 117038448 | 117042260 |
|
Enhancer Sequence | TCTGGCCTTC ATTTACGTCT TTAACAGTGC CTTGGCCAGG TGCGGTGGCT CACGCCTGTA 60 ATCCCAGCAC TTTGGGCAGC CAAGGCGGGT GGATCACTTG AGGTCAGGAG TTGGAGACCA 120 GCCTGGCCAA CATGGTGAAA CCCCGTCTCT ACTAAAAATG TAAAATTAGT CAGGCATGGT 180 GGCGCATGCC TATAGTCTCA GTTACTCAGG AGGCTGAGGC AGGAGAATCA CTTGAACCTG 240 GGAGGCGGGG GTTGCAATGA GCTGAGATTG CGCCACTGCA CTCCAGCCTG GGCAACAGAA 300 CAAGACTTTG TCACAAAAAA ACAAACAAAC AACAACAACA ACAAAACCAG TACCTGACAC 360 ATAAGAGGTG ACCAAAGTCT GTTTGTTGAT TGAGAAGACG GAGGAACTCT GCTCTTCCAC 420 CCTAACAGAA ATGTACTTAG TCAGTCCACA GACCCTCACG AGCATCTTCC CTGGGCCAGG 480 TCCCCTGAGA TTGAAGAGGT AAATCAGAAA GCATCCCTGA CTTTGAGGGA CATAGAAGCC 540 AGTAGGGAAG GGAGCAGAAT TCTCCTGTTT CAACATGTAC AGACAAGTTG CCCAATGCTT 600 TCTCGAAGGT TCCCTCTTTG ATACCGATAG CAACCCCTGA GGATTGGGAA AATCGGAGAG 660 GTAAAGGAAA CTTCCCAGGC TCACACAGTG AGAAATGACA AAGCTGGAAT TTGAACTTAG 720 GCCTGCATGA CTCTACGCAT ACTGCCCCTG TGCTCTGGCA GAGTTGGAAT CCAGGGCTTG 780 GCTGTGGGGC TGTGAGGATG AGCTGGAGGC AGGTGGAAGC TTGATTTTTG AGTGTCGCAA 840 ATACTGGACT GATGACTCGG AACTTGACTT GGTAGTGGGG GGCAGTGGTA GTCTTGTACA 900 GTTGAGCAGG GTTTGTGTGA CCCAGGAGTG CTGGGTCGGT TCAGTTGAAC TCCTTGGGAC 960 CCGTGGATTA GGTGGCCTCG TAGACAAAAT GCCCAAATGC ACAGGCCTGC TGGCATCTAC 1020 CTTGAGCCAA CCAGGTGGTG AGAACTCATG CCTCTGCTGC CATCCCAGTC TCCCTGGGGT 1080 GTCATTTTCA CTCTTCATCC CTCAAGCGGA GAGACTGACG TTGTTACCTA GGCAAAGCAG 1140 CCCAGTTTGA TTCAGGCCTG CTCTTGACAC TGTTTTTCCC CCCTGAAGTG TTTACATGAC 1200 TAACCTAGGA CAGATCCAAG TTAGCCTGCA ACAAACTATG GTTGTGGGAA AATATTTGTT 1260 TCCTAAAAAT AGCACTGAAG TGCCAATCCC CCTAAACAGC TGCAACAGAA TGAACTCACC 1320 AAACTAGAGA AGAATACGAG GGCGCTGAGT CAGCCAGGAG GCTTCCCCCA GGCTTGACTC 1380 AGTGGCGGGC TTGACTCAGC GGCGGGGAAG TAGGCCAAGG GGAATTTAGC AGGAGGGTCC 1440 CGGGCCAGGA TTCTGCATTA GGAACTTGGT CTGCGACCTT TCACCCGCCC CCTGCCCTCT 1500 CTGGTTTTGC CCTTGGAGGG TTTGGAAGGA ATGTGTGCTA AGATTACTTT GAGCTCCAGC 1560 GTTCTAGGGA CCCTTTTTTA GTGAGTGTTG AGTATCATGG CTGTGGAATG GGCAGGAACA 1620 CATGGCAGAA ATAGCCTTGG AACCAGAGTC CTGAGGTTGA ACTTGAGTTT CTGGCTCTAG 1680 TAACCCATTC TCTGTGTGAC TTTGGGCAAA TCACTGCCCC TCTCTGAGCC TTGGTTTTCT 1740 TATCTATAAA GAATAAATAA AACTTAGGGT AGGAAAGCAC TTTATAAAAT GCACCAGAAA 1800 TATAGAAGAT TGTCTTTATA AATTTAGAGG AGAAAGTGAC TAGAGGCTGG TGGTGGCTGG 1860 TGGTGATGGT GAGTGGATGG TGTGGGTGGG GGCAGCAGCA ATGGTAGTGG TGGTAATGAC 1920 GATAATAATG ATGGTGATGG TGGTAGTACT GATGATGGTG TTGGTGGTGG TGATGATGAT 1980 GAAGATGATG GGGGTGTTGA TGGTGGTAGT GGTGGTAGTG GTGACTGTGA TGAGGTGGTG 2040 ATGGTGGTGC TGGTGCTGGT GGCGATGGTG ATAGTGGAGT GGAGGTGAGG GTGATGATGG 2100 TGCTGGTGGC GATGGTGGTG GTGATAGTGA TAGTGGTAAT GATAATGATG ATGATGGGGC 2160 ACTGATGATG GTGGTGGTGA 2180
|