Tag | Content |
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EnhancerAtlas ID | HS026-00507 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:21850920-21852700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:21850986-21850998 | TCTAAAAATAAA | + | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAGATATCA TTGCACCTGT GAATAGCTAC CGCACTCCAG CCTGGGCAAC ATAGCAAGAT 60 CCCATCTCTA AAAATAAAAA ATATAAGAAA AAAAAATGAA TAGAAGCACA AAGGAAGGGA 120 AGGGATCACC CAAGGTCCTA TAGCTCATAC ATGGGTTAAT CCAGAATTGG AACCCGGGCA 180 GCCTTGCTCC AGAGTCCGGT CTCACTTAAT GAGTACTAGA TAATTCTCTG CATGTCAGAT 240 GGGTACACTC TTCTTGAACC TGCTAGTTCT TTTGGAGCCA GATCTGGGGA GGGGGAGCAA 300 GGCAGGAGTT GAGCAAATAG CAGGAACAGA CTGTGTGACA CTTGCTGGGA GGCTCCGAGG 360 CTCCAGCTCC CTGAGCTTAG AAGTGCGGAG TTTATCTATC CCCTGCGCGA TTCCTGGGGG 420 AAGGGAAGGA CAGGCGAAGG GGCATGGCGG GGCAGTCCTG GTGTCTCCAG GACCAGGGTC 480 AGGGGGAGGC CAGAGCAATT AGCCTGGCTG AGGCCTCTGC TAACTCAGAA ACGTAAGTGG 540 GGGATTGGTC CAGGCCTCAC TCCAGGGCTC TGGCCTCGAG CCTGACCCTC CTGAGTTTCT 600 ATCTGAGGCT TCCAGAGTCT TCCTGGGGCA GTGAATCTCA GAGTGCTGGT TTGTGTGAGA 660 ACTTTGTTCT GAAATTTCCC TTTTCAACAA CCAAATCCCT GGGCTGGCCT GCCTGCCCCA 720 CTTCCCCCTC TTGGAGGAAA CGGATGCTTT CCTCTTGGGC GGCCACATGA TTTGAATAAT 780 CAAGTGTTTC CCAGCTGGCC TCTGGCCAAA CGGAGCTCAG CTGGGCAAGG CCCCCAGTTG 840 GGGCACTGAG GCAAGCCTGC CAACCTCCTC ATCCCGCCAC ACGCTCCAGC CACCGAGGGT 900 AAAATACAGG AAAAATGCAT GGCCCATAGA CTTGGCTGGG CCAGGCCCCA GACTATTCCT 960 GTGATGGAGG CAGCGCTTGT CTTGGGCTTT GTCCCATCTA CCTGGAGAAA GCTGAGTGGA 1020 GGAAGAAAAA GGCTGCCCCT GCTCAGGAAA TTCCTGATGG AGCGGCCTCT CCTGGCGTGC 1080 TCACCTGGGT GCTGGCGTCT TGGCACTTGT CAGGGTGGAG AGAGGAGGAA GCCAGTCAAG 1140 AAGGGGAAAG ACGGGTGCGG GAGGACATTC ACTGATTCAA CAAACATCTC ATTAGCCCAA 1200 CTGCCTGTGA GGCCCAGGGT TAGGTGCTGG AATCACAGAT GGATCTGCCC TGGATTTTGC 1260 CTTCAAAGAG TGTGTGTAGG CTGGGCTCCG CGGCTCACGC CTGTAGTCCC AGCACTTTGG 1320 GAGGCCAAGG CCAGTGGATC ACCTGAGGTC AGGAGTTCGA GACCAGCCTG ACCAACATGG 1380 TGAAACCTCG TCTCTACTAA AAATACAAAA ATTAGCCGGG CATGGTGGCG CGTGCCTGTA 1440 ATCCCAGCTA CTCCGGAGGC TGAGGCAGGA GAATTGCTTG AACCTGGGAG GCAGAGGTGG 1500 CAGTGAGCCA AGATGGCACC ATTGCACTCC AGCCTGGGCA ACAAGAGCAA AACTCTGTCT 1560 CAAACAAACG AACAAAAAGA GTGTGTACAG AAATGGTCTT GTAAGCAGAC TCCCCCACAG 1620 AGCCCTAGGT GGTAGAGGAT GAGGGAAAGC ATGAGAGGCC ACCTAGCTAA GCCTTGGGCA 1680 GAATGGCCGC AAAGGATTTC TGGAGACAGC AGATTTCATT TATTTATTTT TTTTGAGATG 1740 GAGTCTCTGT CTCCCAGGCT GGAGTGCCAT AGCGCCATCT 1780
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