Tag | Content |
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EnhancerAtlas ID | HS024-02703 | Organism | Homo sapiens | Tissue/cell | Cerebellum | Coordinate | chr11:61906480-61907700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:61907469-61907484 | TGAACTCCTGACCTC | - | 6.22 | Zfx | MA0146.2 | chr11:61906529-61906543 | GCGGCCTCGGCCTG | + | 6.99 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCTTCCTG ACCTGCCGTG TGCAGTGCCC GGAGCCACAG CGGGCCTTGG CGGCCTCGGC 60 CTGACCTTCT CTCTGGGGAT AAGGAAGCCC CATTTTCTGG GCCAGTAGGC TAAAGAGAAA 120 TTAAACCTGG GGGTGCAGAG ATCCCTTTTG AGTCTGTAGA CTTCACCTCC CACCGTTGGG 180 CTGGAGCTGT CACTGAGTGC AGCATGGGGG GCTGTGGCTG GTTGGGACAG GAAGCAGAGG 240 AAGGGGCTGC ATCGGGGTAT GGATATGAAG AGGCCAGGTC AAGGCCTTGA CCTTGACTCC 300 AGGGGCCAGT GGGAAGAGCT GTGGGCTGGG GATTGAACAC CCCACCTGGC CTCCTGCTTT 360 GCCTCCCCCG CCAGCTCCTT TCTGACCTTT GTATGTCCAT CCTTGTCTAA AGAGGGCTGG 420 AGAGCAGTGG GTTTGGGAGT GTCCCAGGGT CCTGCTCACA TCTCCCTGAG AAGGGTGCCT 480 CTCTCTGGTG GAAAGTGCAC TGTAGCTGTG AGATCTTGAA CACGGCCTCC TCCTCTTTAC 540 GACGTGGTCA GGGACAATGG TCATGCCAGC CCTGCAGCCC CAAGGGCTGC TGTGAGGAAC 600 TTTTGGAGTA AGGTGCACCT TCTCCTAGCA GTGAAACAAA ACAATACTGA CCCTACACCC 660 TCCATGTTGA CCCTGCAGCG GGAGCTGCCC CCTCCTGCTG TCAGGGCCAC ACCAGCTGCA 720 TGGCCCAGGA GGGGTGGAAT TTAGAAGCTG TGCAAGGGGC TTGGAGCTCC TGCTTCTACA 780 AGGCGTCCAC ACACTGTTCT TCGTGTCAGA GGTGGGTGGG GCACGTCTGG GGCTGCCGCC 840 TCGACAGGAC CGTCCCGCCC TGCCTTGCCT ATCATAGAGC CAGGCACTCG CGGGGAGGTG 900 TTCGTGAGCT GGGGGTAGCC AGGCCCTGGC ATCTGTAGAT TTGTATTTTT AGTAGAGGCC 960 GGGTTTCACT ATGTTGGCCA GGCTGGTGCT GAACTCCTGA CCTCAAGGAT CCGCCCACCT 1020 TGGCCTCCCA AAGTGCTTGT AGATTCCTCA AGGCTAGTCA GGGTTAAGGC TGATATGTCT 1080 GCGTTTGGCC ACCCCGGAGC TGCCAGGAAG GGAGCCTTGC CCACTGCCAA GGCTGCTGCC 1140 CAAGGACCCC TTCCCCCTAC ACCCCCATTC CCACCCTGCC GCCGCCATCG TTTCTGCAGC 1200 CTTGCTGAAA TTGCTGTCTT 1220
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