Tag | Content |
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EnhancerAtlas ID | HS024-06343 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr17:76190-78030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr17:77727-77737 | CCCAATTAGC | + | 6.02 | MEF2C | MA0497.1 | chr17:77998-78013 | TTTTATTTTTAGTTT | - | 6.1 | RFX1 | MA0509.2 | chr17:77083-77099 | TGTCACCATGGAAACG | + | 6.13 | RFX1 | MA0509.2 | chr17:77083-77099 | TGTCACCATGGAAACG | - | 6.14 | RFX2 | MA0600.2 | chr17:77083-77099 | TGTCACCATGGAAACG | + | 6.17 | RFX2 | MA0600.2 | chr17:77083-77099 | TGTCACCATGGAAACG | - | 6.31 | ZNF263 | MA0528.1 | chr17:76467-76488 | GCCTTTTCTTCTTCCTCCCTC | - | 6.2 |
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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 |
GH17I000226 | chr17 | 76275 | 77890 |
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Enhancer Sequence | TCTCCGTGAC TGGACCCTCT CTGCTCACTG TGTTGGGATT TCAAGCTGGG GCTTAGAGGT 60 CTTTGTGGTA CAGACCCAAA TCCCATTTCT AATCCACTCT AATAAACACC ACTCGAAAGA 120 AATAAACCAA AGGAAGTCAG CAGTGCCCGC ACCAGCCTTG GCATTTACTG GCAGGGCGGA 180 AGGGCCACAC CGAGCAAACC CTGCTGAGAA GCCCTGGGCC CAACACAAAC ACGGTGTCCC 240 CAAATGTTCC TGGCTTCCTC GGGCTGCAAA GGAAGAAGCC TTTTCTTCTT CCTCCCTCCA 300 TTGAAATGTC ACCGTAAAAC TCAAACTTCG GCTAATTTGC CATTCGATTG CTGTTGCCAC 360 CTTTCTCCCT GCATAGCAGC TGTGATTGTC AGTCTTCCAG GTCTATTCAC AAAGATTTCA 420 GACTCATACA TCTGGCCCTT GCTCTTCCAT CCTCAACATA ACACTCTGTG TGTCTGAAGG 480 CTGATACATT TTTTTTCTCT CTAATTCTCC AAAGGCTGAG TCTGGGATGG CTCACCGACG 540 AGCCCTGTAT TCTGCCCACG CCTGGTTTTT CAGATGGAAG ATGCGAGTAC ACCAGGGAGA 600 AGGCTGTCCC AACAGCCTTT CGGAGGAAGA AGTATCATGG AGTCACCCGG GTGCCGCCGA 660 GAGGCAGGGG TGGGGGAGAA GCTCCCCTCC TGGGCCCCTC CACAGGGGCC TGAGCCACTT 720 GCTGGGGACC TGGCATCCCT GAGGCTTCCC CACTGCAGCC CAGAAGGGCT GCCTGCTTGC 780 CGGGTGCTCA TCCTCAGCAG TGGCCAGCCC CAGCGCCAGC CGTGCCCACT TCTCTGGGGA 840 GAGGCCAGCT TTTCTTTCCC CCTGCTCACT CTTGGCTGGG TTTGCAATTT GACTGTCACC 900 ATGGAAACGC AGGGTTTTGG TACACGGAGC GGGGGGAAGA GTCTTTCCTT CTGGAAACGC 960 TTTCTTGACT GCCTCAAAGG ACATGGGCGG CAGCTGTCCT GTGGAGAGGC CTGGCCTGGG 1020 ATGGTCCAGG GGACAGGCGT CATGCTGGCC GTGTGGCCTC ACAGCACTGC GCTGGGGATG 1080 TGGGGGCCCT GCTTCCAGGC TCTGCTCAGC CACCACCTGT CTCTGTGGCC CCAGGCATCT 1140 CTCCAGGCTT CACTACAAAA ACACAGGGGC TGACCCAGGC ACCCACTCTG GGTCTGAATC 1200 CTGGGATTTA ACCTTGGGTC AGCCCATGGG TGGAGACAGC CCTGGTGCCT CTCCCTGGTC 1260 GGGGTGGGGA GATGCTCCCA CTGGGCCACA GAGCATTGCC GCCCGGCACA AGGACAGCCA 1320 GCAGCCTGAG TTTGGGAGGC ACTTGTGAGC TACGGCCACT CTGCTTGGAG GCTCCCAAAG 1380 CCCCCAGAAA TTATGGGAAT TATAGAGGAA GAGAGATATT TTCAGCAAAC ATTCTGCCAA 1440 GGCAAAGCAG ATGGTGGAAA ATTTTGCATA CTAAAAACAA AAAAAAAATT CTCTAATGTA 1500 AAGGAATGAT GATAAGGCCC CTGGGAGTGT AGACACTCCC AATTAGCCGT CTCCAGCCCA 1560 CCAGGCAGGC ACAGCTGCAG AGACGCAGGA CTGTCTGTCC CTGCTGGGAC AGGGGACGGC 1620 TGCTCCACCT GCACACAGGG TAGGGTCCTT GGCCTGAAGT CCCACTGAGA TGTCTCCCAA 1680 GGCTGGGGCT CCATCTTGGT GGCAGCTGGA GGGGAGCCTG GGGTGGGGGA GTCACCGGCT 1740 CTGAGACTTG GGTTGGTGTC CTGCCTCTGC CACCTCCCAG TGGTATAACT TTAGGCCAGT 1800 TTCCTATTTT TTATTTTTAG TTTTTGTAAA GACATCATCT 1840
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