Tag | Content |
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EnhancerAtlas ID | HS105-12467 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:587460-588530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:588032-588043 | GGATGACTCAT | + | 6.62 | JUN(var.2) | MA0489.1 | chr11:588029-588043 | TGAGGATGACTCAT | + | 6.08 | JUNB | MA0490.1 | chr11:588032-588043 | GGATGACTCAT | + | 6.62 |
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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 |
GH11I000586 | chr11 | 586259 | 589150 |
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Enhancer Sequence | CAAGGTGAGT TCACCTCTGG TTGGGTGCTT CCTCCCTTCA GGATGGCCTC CCTGTTTATA 60 GGTGACCCAG CCTGTGTTCA GCCTCTTGTG AGGTTCTAGT TGTCTGCTCT GCGGCTGACC 120 CTGGGGCCAC AGGATTGAGT CTGGCTTGGT CTTTGCTTTG TGAGCACCAT GGCTCTTGGG 180 GGTGTGGGTG AGCTCATGTG AGGCGTTTGT GGTGTATTGG TCAGGGGCAG GAGAGAGGAT 240 GGCCGTGGGT CTCCCAGGAC CAGCTGCAGA AACCCTGGTT GACATAGGGG CCATCTTGGC 300 CTGCAAGCCA GAGGCAGGTG TGCTGTGGTG CGTGGTCACT TTGCTGCCTT GACATGTGGT 360 TCTCTCAGTT GATACAGAAA ACACCGGTAC GATTTGGCAT TCATTCACAA TAACTGGCAT 420 CAAAAGAGAC TGTCCTTAAA ACAGGTGAAT AGAGTTTACC GTAAACGTGC AGTGTATTTT 480 ATATTTCAAA ATGAACTTTT AGAAGCAGTC AGCTCCCCCC TCCCTTTCTG AATATTGTGA 540 AAAATGTCAG AAAAGGAGAG CTTGCAGTCT GAGGATGACT CATGAGTCCC CGACCTCTGT 600 ACTCAGGGCT CAGCTCCGAC ACCACTACCT CTTGACTCCC TCCCCTCCCT GCGATTGCAC 660 CAGCAGCCCG TGCTGTCCCC GGCTCTCTTC AGGACCGTGA CCTCACCCAG GGTTCCTAGT 720 GACTGGGTCC TCCTGTTCTG TTTCACTGAG TAGCTGAAAA CTGCCTGTAT GCTTAGTTTG 780 AAGCAGGACC CAGACATTCC TCATGCTGCT GGTGGTGGCA GGCTGTGATG TCACCCAAAG 840 TCTGGCTCTG GTACTTCCTG TTCCTGTTCT GTTGTGGTGG GTCCACAGCA CACAGTAGAT 900 TCAGACTTAG ACTTTTCTTT TTTTTTTTGT TTTTTTGAGA CGGAGTTTTG TTCTTGTTGC 960 CCAGGCTGGA GTGCAATGGC GCGATCTTGG CTCACCACAA CCTCCACCTT CCGGGTTCAA 1020 GCGATTCTCC TGCCTCAGCC TCCCGCGTAG CTGGAACTGT AGGTGCCCAC 1070
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