Tag | Content |
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EnhancerAtlas ID | HS101-44970 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr9:27184470-27185480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr9:27184763-27184774 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr9:27184763-27184774 | GGTGACTCATG | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGAGGGAGG AATATGTAGA ATGTACCATT ACTAGGGTCC ACGTTTCAAT GTCCCTGATT 60 CCACTCAAAC AACCCATCAG GTAGAAGAAG CCAATTGATG GCTTCCAAAA TCTTATTGGC 120 TTTTTCATGA GTTAATGAAA GTAATGGCTA CTATTTAGTA AGGTTGGCCA TAACTATATG 180 TAACTTCTTA CTTAACATTG CCTAGTGTCT CTTTTTTTTG GCGGAAGTGG GAACTGGCTG 240 GGTGAAGTTA AGTAACTAAG GAATTGGTCA AAAATGGCAA AGAGGCCAGA TACGGTGACT 300 CATGCCTGCA ATCCCAGTGC TTTGGAAGCC TGAGGTGGGA GGATCACTTT AGGCCAGAAA 360 TTTGAGACCG GCCTGGGCAA CATAGCAAGA CCCCATCTCT TAAAAAATAA AAAAAGAATT 420 AGCTGGACAT GGTGGCATAT ACCTGTAGTC CCAGCTACTT GGGTGAGGTG GGGGGATCAC 480 TTAAGGCCAG GAGTTTGAGG CTGCAGTGAA CTATGATCAC TCAACTGCAC TCCAGCCTGA 540 GCCAAGGAAC AAGACTTTGT TGTCTCTCAA AAAAAAAAAA ATGGCAGAGG TCCATCTCTC 600 TTCAGAACCC TGGATTTTTC CAGTACTCCC CACTTGACAG CCTCTCAAAC ACTTAGGAAG 660 TCACTTTGTC CTCCCACGCA GCCATCTCTG TGTTAGATAG GAAAGGAACA AATCTTATGA 720 GGAGGAGTTT AAAAGAAATC ATGCTTCAGG TGTCTTGCTT GTAAGTGTTT ACCCCGTACT 780 CCTAAACACA CAAATACAAC AGCAGGATCT GACAGGGCAT CAATCCAAAA TAAACTTTCA 840 GGGCTACTAC AATAGCTTTG GAAATAAGCC AATAATTATA TTAGCATTAC ATTTAGCTTC 900 TTGATCTCTC CTAGGAAACT TCTTATTAAA CAATGAGATG GGGTCAATGT TATGGACCTT 960 TGCGTTTATG CCTCCCTAGA AGTTTTTATT TTTTTGTATT TGACCTTTTC 1010
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