Tag | Content |
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EnhancerAtlas ID | HS183-13231 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:116026770-116027910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr9:116027078-116027090 | AACCCGGAAGTC | + | 6.14 | ELF1 | MA0473.2 | chr9:116027078-116027090 | AACCCGGAAGTC | + | 6.74 | ELF3 | MA0640.1 | chr9:116027078-116027091 | AACCCGGAAGTCA | + | 6.27 | ELF4 | MA0641.1 | chr9:116027078-116027090 | AACCCGGAAGTC | + | 6.18 | Mafb | MA0117.2 | chr9:116027472-116027484 | AAAATGCTGACG | + | 6.74 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATGCAAGTC TTTCTGCCCA GAGTGATAAT GCAATAAGCT AGTCTTTTCA TAGTCTGCAT 60 AGAGTCTGGC CATTACCATC AGTTTTTAAG ATGTCCATAT TGTGGCCGGG CGCGGTGGCT 120 CACGCCTGGT AATCCCAGCA CTTTGGGAGG CTGAGGCAGG TGGATCATGA GGTCAGGAGA 180 TCGAGACCAT CCTGGCTAAC ACGGTGAAAC CCGTCTCTAC TAAAAAAAAT ATTAAAAAAT 240 TAGCCAGGCC TGGTGGTGGG CGCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCAGGAGA 300 ATGGTGTGAA CCCGGAAGTC AGAGGTTGCA GTGAGCCAAG ATTGCACCTG GGCAACACAG 360 CGAGACTCCG TCTCAAAAAA AAAAAAAAAA AAAGATGTCC GTATTTTAGG TGGTATGATC 420 CTTTTAGGTT TTCATCTCAC TCTCCCCCTA CTCGACTTAA AATGACATGC CTAGTACATG 480 CCAGAAGATC CATGTGACCT TCTGCACAGG AGACAGGGTC TTCATGAAGC CACAAGTATT 540 TCAGTATACT GAGGATTCCT CAGTTTAAAA GCCAACTTTT GTCACATCAT AATCCCTTCC 600 CTGTGTCTGC TGTTAGGCAA GAGGCTCTGA GCTGGGCCTA TAAGAAGTTC ACCGCCCAAC 660 CTTGAGATGC ACAGTGACCC TGCCAGTCCC TTTGGTAATG CCAAAATGCT GACGTTACTT 720 GCTCTTCCCA CTGGCCCCCA GTGGGCATCT TGCCATCACC ACCATTCCTA GTCTCTTCCG 780 AGTGTAGTGT CATGAACATG GACTTAGAGG AGTCAATGAG TTTGGATTCT GGTTCCATCA 840 CCTACTAGCA GTATGACCTT AGGAAGTTAG TCTAATGATC CCTAAGCCTT AGTTTTCTTA 900 TTTAGAGATG GAGTCTCACT CCGTCACCTA GGCTGGAGTG CAGTGGTACA GTCTCGGCTC 960 ACTGCCACCT CCATCTCCTG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG 1020 GGGCTACAGG CACACACCAT CATGTCTGGC TAATTTTTGT ATTTTTAGTA GAGATGAGTT 1080 TTTGCCATGT TGGCCAGGCT AGTCTTGAAC TCCTGAGCTC AGGTGATCCG CCCGTCTCGG 1140
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