Tag | Content |
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EnhancerAtlas ID | HS024-04092 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr12:133144110-133145830 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr12:133145538-133145551 | CGCAGCTGTCCCC | + | 6.57 | Myog | MA0500.1 | chr12:133145537-133145548 | CCGCAGCTGTC | - | 6.32 | RREB1 | MA0073.1 | chr12:133145781-133145801 | GGGTTTGGGGTGTGCGGGGG | - | 6.06 | ZNF740 | MA0753.2 | chr12:133145800-133145813 | GTGGGGGGGGCAG | - | 7.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 133145140 | 133145240 | chr12 | 133145532 | 133145736 |
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Enhancer Sequence | AGGTAAGTGG GTCCCCTCGG CCCAGCTCCT GGGCCTCTGA AGAGACACAA TGCGCCCTGC 60 GTCTTGGCGG CAGGACATCC CCCTGAAGTC AGGGGAGAGA TGGTCTTGGC ACCTGGGGTG 120 CAGAGCTGGG TGGGACCAGG GTGCTGGGAT TGCTGGGAAG CCCCCAGGAG CAGGGGAGAG 180 TAGACGAAGC CACTGAGCCC TAGGCAGGGC CTGGGCTCCG CTCGTAGCAG CGGCTCCCAG 240 AGTGGAACCG TTAGGAATGT GTGCTCTCAG GCCCTCCCCA GGTTCGTGGG GTCAGATGCT 300 CGGTACTGAA GGGCCACCTG CCACGAGCAC CACAATCACC TGTGGCTGCT GAGTTAAAGA 360 GAAACGGGAC TGAGACTCAC TTCCCTGGCT CTGCTGCCTG CGCGCCTCTG TGGTGCAGTG 420 GAGGGGCCTG GATTGCTGTT CCAGGCCAGG CCTTCGAAAC CTGTGGCTGT GAGCTATGGG 480 ACAGGGTGTC TACAGGCCAG CAACCCTCTC CAGAGGGGGT AGCCCCGGCG TCTTAGGGGC 540 CTTCGTAACC TGTGGCTGTG AGCTGTGGGG CGGGGTGTCC ACGGGCCAGC AACCCTCTCC 600 AGAGGGGATA GCCCCAGCGT CTTCTTAGGG CCTCCCTGGC GCTGGGATCC TGGGATTCCC 660 ACACCAAGGC CTAGGCGGGC AGCATCTCCG GCAGGGCCAC GGGGTCTCGG CTCCTGCCTC 720 CCTGGGTTTC CAGCTGGAAC CACCCTTTTG CTGGGACGGC TTCATCCGGA TGTGATTGGA 780 CAGGACAGGC CCTGCCAATG CCGGCAAGGA TGGGCCCTAC TGCCCTTCAG CAGGCATGGC 840 CTTCACCTGC CTTCAAGTTG GAAGCCTGTT CACATCAGAG CATCACAGCA AAGCAGGCGC 900 AGATGGGGTG GTGTCAGAAG GGGCGTGCAT GGGACGGGCC CCGGTAGGAG AGGCAGCTGG 960 CTTCGCAGAC GGTGTCACGC GGGGCTGCTG AATACTCAGC TCACTGCCGC GGCTGCTGCC 1020 GCATCTGGAC GGACAATGTC CCAGTGAGGG CTGGAGGTGC TAGAAGGGCA CAGGAGGCCC 1080 CGCACGTGGG GTCTAGTCCA GGTCTGTGCG GCCCAAGCCT CTTTCCATCC TGATCACAGC 1140 TCTTACTATA TGCAAGGCTG GCTTGGAGAT GTGGGAGAGA GGAGGAGAGG TCCCGTGGGG 1200 CTGACCCAGG GAGCTGGGAA AGCCGGTGGA GATAGTGCCC GTGGGCTCCC TCTCTCCTGT 1260 GTCCTCCGCG CAGCCTCTCT GTGGTCGCTG GGTGGTGGCT GCTGTGGAAG GCCTGGCCCC 1320 AGGTGAAGAG TGAAGATGGG GCTGCTTCCT GCTGCCTGTT TTCACCTGGG AGGAACTCCT 1380 TGAGGCCCCA GAAGACCAGG CCCCATGGTC ACATGGGGCA GGGACGGCCG CAGCTGTCCC 1440 CATGGGCCAT GGCTCACTGT CCCAAGGCCT CAGGAAGGAA GCAGGGTCTG CCGGGGACGT 1500 GAACAGGAGG CATGCGGCAC GTGGAACGTT GTTTTGTTTC TCCTGCGAAA CTGGCCCCCT 1560 GACCGTGGCA GCTCCTGACC CCAGGCAACA GGAGCTCCAC CACATGGACG CTGCCCTCTC 1620 CTGACTCCTG GGGACTTGAT CTGAGACCTG CCCGAAGGGG CCTGAAAAGG AGGGTTTGGG 1680 GTGTGCGGGG GTGGGGGGGG CAGGCCCCAG GGGCTCAGAG 1720
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