Tag | Content |
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EnhancerAtlas ID | HS043-10070 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr12:48469240-48470860 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr12:48469762-48469777 | GTTCCAAAAATAGTA | + | 6.39 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAACCTGTT AGAAAAATCA CAAGGAAGTA ACCAGACTAG TCAAAATCAG AGTGGAGTAT 60 CTTGCCAACA GTTTCCTATT TTATTTAAGT GCAGGTACTT TCCAGAGACA ATATTCATCT 120 CCAACATGTA TTTATTTTTC CTGTAAGACC CAATACTACA TTTAGTGAAA ACCATATACT 180 TCCTAACATT CATTCATTGA CATGAACACC TACTATGCTC CAGTCACTAA AGATAATGAA 240 TGCATCAAAT AAAATAAAGT TCCTGCCCTT GTGGAGATTA TATTGCAGTG AAAGGAATCA 300 AACAAAAAAC CAGTCAGGTA GTATGCAGAA AATTAAAGGG TAAGAGAATG GAAAGTGATG 360 GAAGGAGAGC AGCAGGAACA GGTAAGATTT CTCTAAAAAA AAGTGATATT TCAGCAGAAA 420 CCTAAAGCCA AGGGAAGAAG TCAGTCCTAG AAATATATAA AAGAATATTC CAAATAGAGG 480 AACAACACAT GCAAAGCCCT GAGAGAGGAA GGTGCTTAAT GCGTTCCAAA AATAGTAAGG 540 TCCATGTGAA TCAGAAGAGT AGGAAGAAAT GAGATCACCT GACACAGAAC CAGATTACAT 600 AAGGACTTAC AACTCTGGTA AAGCATCAGT TCTATACAGG TCCCCTGACT CAATGGGCTA 660 TGTTCACTAG CACTTAGTAA TATGCCCTGG CAATTTATTT TTAATCTTAT ATACAGTTTA 720 ATACAACCAC CAATCCTCAA AACATAATTT TAAACATTAT GTCAGTGTTA GCACCATCTC 780 GTACTGTGAT ATTTCGATAT GTGCTGGGAC TACAGGCGCC CGCCACCACG CCCAGCTAAT 840 TTTTTGTGTT TTTAGTAGAG ATGGGGTTTC ACCATGTTAG CCAGGATAGT CTCGATCTCC 900 TGACCAGCCC AGGCTGGAGT GCAGGTGCGC CATATCGGCT CACTGCAACC TCCACCTCCT 960 AGGTTCAAGT GATTCTCCTG CCTCAGCCTC TGGACTAGCT GGGACTACAG GTGCACGCCA 1020 CCACACAGAG CTAATTTTTT TTTTTTTAAT TTTTAGTACA GACAGGGTTT CACCATGTTG 1080 GCCAGGCTGG TCTCGAACTC CTAACCTCAA GTGATGCGCC CACCTTGGCC TCCCAAAGTG 1140 CTGGGATTAC AGGCATGAGC CACAGCACCC AATATGTAGT TTTTGCTTTT TTTTTTTCTT 1200 TTTTGAGACG GAGTCTCACT CTGTCACCAG GCTGGAGCGC AGTGGCACGA TCTCTACTCA 1260 CTGCAACTTC CACCTCCCTG GTTCAAGCAA TTCTCCTGCT TCAGCCTCCC TAGTAGCTGG 1320 AACTACAGGT GTGCGCCACC ACGCCCAGCC ATTTTTTTTT ATTATTTTTA GTAGAGACGG 1380 GGTTTCACCA TGTTGGCCAC AATGGTCTCG ATCTCCTGAC CTCGTGATCT GCCTGCCTCG 1440 GCCTCCCAAA GTGCTGGGAT TAAAGGCGTG AGCCACGGCG CCCAGCCACC AATTTGTAGT 1500 TTAACACTTG GTCTCCTTCC ACCCTCCCAT CTTGTAGTCC CCAGTGTCCA CTATTCCCAT 1560 CTTTATGTCC ATTTGTACCC AATGTTTAGC TCCCACTTAT AAGTGAGAAC ATGCAGCATT 1620
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