Tag | Content |
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EnhancerAtlas ID | HS139-42530 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr4:176921260-176923450 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr4:176921880-176921890 | CTCAAGTGGT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 176922084 | 176922777 | chr4 | 176922288 | 176923378 |
| Enhancer Sequence | CTTTTCTCTA TTTCGCTCAC CTCTGGCTTC CTCACTTGCT TCCTCTACTT CCATCTAAAG 60 AGAGTTCAGG AATATTTTTA ATCTGTCCTA CTAGGCCCCT GACTACGTAA GTTTTTGGTG 120 ACCTCAATTA CAACAGGAAA AATGTTATCC ACTTCTGGCA GTAGAAGGAA CAAACAAATT 180 TTAGGTATCT GTCAGATTAC AGACAGGAAA GAGAACTTCT AAGAGTTACA GACCAAGCTT 240 TGGATCCTGA CAACTCAGCT GTTAACTCCA CACCATCCCC CACAACAAAA TCTTCCTATA 300 ATTAGGGATG ATTGTTAATT ATCCATGGGC ATTGAAGCAA AATCCAGGAC AAATTGTTTT 360 CACTATAGTA AGGAAATGGA AATTAAAAAT AATTAAGTTT GAAATTATGA ATACCTTACC 420 TTTGATAGCC AGTCCTCTCG AGCTTGAGGT TACAAGGGTA AATTATGTAA TTCTTTCTAG 480 ACATTTTATT ATGTTGGATC CAAATGGCAT TTTAATGCTT TTAATACAGC TAATGAATAG 540 ACTACATCAA GTCAATTATT TTGACTTTCC ATTTCTGACA GCTTTTCTCC TGTGTGAGCA 600 TAGAAACAAG AGTTTATAGG CTCAAGTGGT CAAGTAGAAC AGCAAGTGTT GGGTTTAGGA 660 GAAAAATTTA AAATATTCCG GACCTGTCTT TCCAATGGAA CACAACACTT AACAACCAAA 720 TAAAAAAAAG AGCCTGAAAT ACTCTCTGCC ACACTTGGGA AAATGTTTTA TCTTTCTTTT 780 TTAACCTGAA AATACTCCTT CCTTTTCAGA AAACATTTAA AGACAGTCCT TCTTAAGACC 840 ATTTCCAACA CTGTTTATAC AAAGGCCCTA AAAATGGGTC CTTCTAAGAC ACTTCCAGGG 900 GTCAAGCAAG AAGAGACTAT GAAAGTCTTG ATCACAGCTA ACATTCATAG GCAAAAATGT 960 CCTCAGCTTT CTCTTTTTTC CTTTCTTCCA AGTTGGCTAC TGTCTATAAA CTCCAGAAAT 1020 TAGTAGTCAA AGCATCCCCT AACCCTTGAG CCTGTGGGAA TACAGGAATT TCAACCCGAG 1080 CACGTCAGTC CCCAAGGCCT CCTTTACTCT TGGAGAAATC CCTCACAACA AAGGACAAGG 1140 GAGAAGCAAG GGGGAGGGGC GCCCAGTGGA CTTGGCTGGA AGAAGTGAGC GGGCTGGGGT 1200 TGGAAGAGTA ACTCGGGCTG CGGGCTGAAC GCAGTCGGCA ACCGCGGAAG AGCAGCATCT 1260 CCCCTGCGCC TGTGGATACG CCAGTCCAGG GATGGCGAGT GCTTTCTCCT CCCCAGCTTC 1320 TCCCTCGCTC TTCGAGGTGA CTCGTGGGAC CCTGCGTCCT AGTGCTGGGT GTGAATCGGC 1380 TATTTCACAC CCAGTTCTTC CTCCCCTCCG CCACACGCAG TCACATTCCT GGAGCTATTC 1440 CAAGCTGCCT CCGCTAAGCA CCGAATAAGC GGACCCTGCC TGGAAACTTG AGCGAAGCTG 1500 AACTGCGCCG AACTCCACCG TCCAGTGACC CGAGCCAGTG TGGACGCCCT TTTAATCACG 1560 CTGTTTACCC AGGTGGAATT TAGGAAGAAT CAGCCTTCAG CCTCAACCTC AAACCTTTTG 1620 TGCAAATGGG CACTTCGTTT GGAAAGGGAC TAGAAATTGT CCCCAGTCTG GCCCTGCACC 1680 AGCACCTTCC TCTGCTCAAA CCTGTACAAA GTGGAAGTTT TAGGAAGTTT CCATTTCTCG 1740 TGCCCCGTTT CAACTTGCTC CCCAAAGAGA ACATGAAAAC GTGGGAACTC GGGAGGACAG 1800 AGATCTCCCT GTAATCGCCT CGCTATTCGG ATCCTGGGTC TCTTAGTCTT TCTTTATTTC 1860 CCAAATACCG CCCCCAGCAC GGTAGACCGG ACCCCCAGGC TTGGGTCCTG GGGCCGGCGC 1920 AGAGGATCAG CGCCCAAGCG CAGCCCCCCA CCCTCCCGAC CCACTGTAAA CAGTCGGGCA 1980 CCCTCCCTCG CCTCCAGGTG CCACCCCATC GCCATCGCCT CTCTCCCAGA AAAAAAAGTC 2040 CGGAGACAAG AGGGCGGGGG GCGGGGGACG CCAGGCGCGG GGGGAACAGA GCTGGGAAGG 2100 ACGCAGTCTG AGGCCGAGGA ACATTCATTT TCTTTCTATA ATGCCCATTC CCGAGGCCGA 2160 GCCTTTGGGC GAGGTGTACG CGCCCGCCCG 2190
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