Tag | Content |
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EnhancerAtlas ID | HS037-29512 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr4:176921850-176923450 | 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 | TGTGTGAGCA TAGAAACAAG AGTTTATAGG CTCAAGTGGT CAAGTAGAAC AGCAAGTGTT 60 GGGTTTAGGA GAAAAATTTA AAATATTCCG GACCTGTCTT TCCAATGGAA CACAACACTT 120 AACAACCAAA TAAAAAAAAG AGCCTGAAAT ACTCTCTGCC ACACTTGGGA AAATGTTTTA 180 TCTTTCTTTT TTAACCTGAA AATACTCCTT CCTTTTCAGA AAACATTTAA AGACAGTCCT 240 TCTTAAGACC ATTTCCAACA CTGTTTATAC AAAGGCCCTA AAAATGGGTC CTTCTAAGAC 300 ACTTCCAGGG GTCAAGCAAG AAGAGACTAT GAAAGTCTTG ATCACAGCTA ACATTCATAG 360 GCAAAAATGT CCTCAGCTTT CTCTTTTTTC CTTTCTTCCA AGTTGGCTAC TGTCTATAAA 420 CTCCAGAAAT TAGTAGTCAA AGCATCCCCT AACCCTTGAG CCTGTGGGAA TACAGGAATT 480 TCAACCCGAG CACGTCAGTC CCCAAGGCCT CCTTTACTCT TGGAGAAATC CCTCACAACA 540 AAGGACAAGG GAGAAGCAAG GGGGAGGGGC GCCCAGTGGA CTTGGCTGGA AGAAGTGAGC 600 GGGCTGGGGT TGGAAGAGTA ACTCGGGCTG CGGGCTGAAC GCAGTCGGCA ACCGCGGAAG 660 AGCAGCATCT CCCCTGCGCC TGTGGATACG CCAGTCCAGG GATGGCGAGT GCTTTCTCCT 720 CCCCAGCTTC TCCCTCGCTC TTCGAGGTGA CTCGTGGGAC CCTGCGTCCT AGTGCTGGGT 780 GTGAATCGGC TATTTCACAC CCAGTTCTTC CTCCCCTCCG CCACACGCAG TCACATTCCT 840 GGAGCTATTC CAAGCTGCCT CCGCTAAGCA CCGAATAAGC GGACCCTGCC TGGAAACTTG 900 AGCGAAGCTG AACTGCGCCG AACTCCACCG TCCAGTGACC CGAGCCAGTG TGGACGCCCT 960 TTTAATCACG CTGTTTACCC AGGTGGAATT TAGGAAGAAT CAGCCTTCAG CCTCAACCTC 1020 AAACCTTTTG TGCAAATGGG CACTTCGTTT GGAAAGGGAC TAGAAATTGT CCCCAGTCTG 1080 GCCCTGCACC AGCACCTTCC TCTGCTCAAA CCTGTACAAA GTGGAAGTTT TAGGAAGTTT 1140 CCATTTCTCG TGCCCCGTTT CAACTTGCTC CCCAAAGAGA ACATGAAAAC GTGGGAACTC 1200 GGGAGGACAG AGATCTCCCT GTAATCGCCT CGCTATTCGG ATCCTGGGTC TCTTAGTCTT 1260 TCTTTATTTC CCAAATACCG CCCCCAGCAC GGTAGACCGG ACCCCCAGGC TTGGGTCCTG 1320 GGGCCGGCGC AGAGGATCAG CGCCCAAGCG CAGCCCCCCA CCCTCCCGAC CCACTGTAAA 1380 CAGTCGGGCA CCCTCCCTCG CCTCCAGGTG CCACCCCATC GCCATCGCCT CTCTCCCAGA 1440 AAAAAAAGTC CGGAGACAAG AGGGCGGGGG GCGGGGGACG CCAGGCGCGG GGGGAACAGA 1500 GCTGGGAAGG ACGCAGTCTG AGGCCGAGGA ACATTCATTT TCTTTCTATA ATGCCCATTC 1560 CCGAGGCCGA GCCTTTGGGC GAGGTGTACG CGCCCGCCCG 1600
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