Tag | Content |
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EnhancerAtlas ID | HS139-03997 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr1:182326720-182328080 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:182326865-182326877 | AAACAAACATTT | - | 6.27 | MEF2A | MA0052.3 | chr1:182327256-182327268 | TCTATTTATAGC | - | 6.62 | MEF2B | MA0660.1 | chr1:182327256-182327268 | TCTATTTATAGC | - | 6.52 | MEF2C | MA0497.1 | chr1:182327255-182327270 | TTCTATTTATAGCAC | - | 6.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAAAGTGTTT GGAAAAAAAA CTTCTGCTGA GCAATCTGGG GGAGAGAATT TAAAAAATTA 60 AGAAAAAAGA AAAAGTTTGG ACATCATGAC ATCTGGGTGC TGTTGCACAG TCCTGGTAAC 120 TACTCCTAAC CTAGTTACAT GAGAAAAACA AACATTTTTT GTTAAGCACA CAGTCAGTTT 180 TCATTCCATG CTGACAAATG CAATTTAATG AACTCACTGG GGTTTAGGAA ACCTCATCCT 240 TAGGAAGGAA TAGAGATACC TGAAAGGAGT TAGCTTGCCT AGCCTGGCTT TGAAAATAGG 300 AAAGAATTGC TCTTCCACCC TAACTTACCC TAGGATACCC TGAGGCCCAG GGCATGTGCC 360 AGCCCAGAAG GAGCCACAGC CCTCAAAGAC AGAGGGAATC ATGAAATGGA GCCAGGGGAT 420 TTATGGGGCT TCAGATTCCC CTAAGATCCC CCAAGCAAGA GTAGGGCAGC AGAACGGCCT 480 GCTAGAGGGT TGAGCGTTGG CAACTTGACT CCAGTGTTTG GGGGTATAGA TCCCATTCTA 540 TTTATAGCAC CAGCAGGTGG GCAGGAGGAG GGAGTGGTGC TCTTGGCAGC TGTTTGTTTT 600 GAACCTGCCA AGGCAGCTCC CTGAACATTT GCTTAAAAAG CAGAAGAGGG AAGAGTAGAG 660 TTGGGATGGG GATGCAGGAA CAGAGCTTGG AAGAAAGAAG AAAAAGAATG GCACACACGT 720 TCGAAATGGA ATTGCAGGGT CTAAACTCTT ATGAGGGTCA CATTTCCCCA AGGTAATCTT 780 GATGTTTTTG GACGGGCCAA ATATCCCCCA ACATGATTCC CTGAGCCTTG CAATCCTTTG 840 GGCCTGGGCT TGGCTAGACT AGAGTTAGAG GCTGTTTGAA AGTCAAAAGC AGTCAGAAGA 900 GACAAGAGTG CCAGGTCACT GACACTAAGG GGAAGAAGAT TTTGAGAAGA AAACTGGGCC 960 AAGCTTTTCA GAGAGGCAGG GAGGTTGGGG GTGTGACCAG CTGGCTTGCC AGTGGAGGTG 1020 GCTGGGGTTG ACCATTCTTT CTTAAAATCT AGCAGTAAGC AGAAGAAAAA AAATATGGTA 1080 ATATCTTGAT AAGTGATGGA GTCAAGGAAA AAAGGAAGAT ACGCCTGTCT AGGCCAAAGA 1140 AATATCTGGT AAGACTGAAG GAGCAAGCTG AGTGAGAATT TTAGATTGTG ACAGGCTACA 1200 GTCATGCTCC TCGGCCACCT CCCAGGGGAC CTATTGCCTC TTTTTTGCTG TTAGTGTCCT 1260 TCCATCTTTT TTACTTTTAG GATCTCCCAG AGGATATAAA CTTCACTGGA CACTGTTTAT 1320 GTTTGTTGTT GTTGTTGTTA TTTATTTTTT TTCTTTCTGT 1360
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