Tag | Content |
---|
EnhancerAtlas ID | HS139-32207 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:239509680-239511170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr2:239510763-239510775 | GCTAAAAATAGT | + | 6.11 | MEF2C | MA0497.1 | chr2:239510761-239510776 | CTGCTAAAAATAGTA | + | 6.1 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I238600 | chr2 | 239509016 | 239511152 |
|
Enhancer Sequence | AGGAAGGAAT AAGGAGGAGT CCCGTTCAGT GGAGAGCAGG CTGTGCGCTA CCCCACTGTG 60 GAGAAGGGTT GCACAGGCAC CTCCAGGGGT ATGTTCTGGC CACTCCGTGC TGCAATCTTG 120 GGGCTGCCTG CCCATCCCTA ACATGTTAGA CTCAGACTCA CTGCTCTTGC ATCGTGCCCC 180 AGCCTCCAAG GAAAACCAGC CAGCAACCAC AGCGCCGGTT CTAGGGACCC TCCTGGATCA 240 GGCCCACGTG GTTACTGCCC CTCGGGCCTC AGATCAGTGG TTCTATCCCC AGCTCACCTG 300 TCCCTACCCG CCCGTGGTCT GACTTCTGCT TCTGGGTTCT GCTCCTCCTT TGGGCCTCTG 360 ATCCTCCTTT GGGCCTTGCC CTGCAAGCTG CTTTGCTCTG GTTGGTCTCT GAGAGGAGCC 420 CCTGCCCCTG GTCCAGTGCG GAAGGAGGAG GCTAGCAGCC AGCGCTTTCC CGCAGCTCAC 480 TTGCTGTCTG TGGGCCGACA GGAAGTTCTT CATGGGGAAA GCCAAGAAGC CAAGACTCAC 540 ATAGCAAAGC CTCCGTTTGG AAGCCGGTGT TAGTCCTTTC TCCTTGAGGA GCAGTTTCAG 600 TCAGTGCATC ACTCCAAATG GGTTTGGTAA CACTGAGCTT ATGGTACAAT GAAAATCACT 660 CTTGCCAAGA GAGCAAATGC AGATGAAAGG CAGGGTGAGT CACACGGGCT CTCCATGTCC 720 CTCTTGCTGC ACCCCCAGCA GCCTTTGACA CAGGAGCCAG CCACAGACAG TGCTGGACCC 780 CAGCACGTTG CCCCAGACTA TGCAATGTCC AATTTCTCCA GGCCTCACCT TCTAGGACCC 840 ACTTCCCGAT GCCTGGACAT CTCATTGTTC TTTTCTGGTT TACTTCCAAG CTCTGGGGAA 900 TCCACCCTTG GCTAGCATCA CTCAGAAATT GCACAACTAC CATTTTAAGA CAAGATTTTA 960 AGAGCTGTTT AATTTAACTT TTAATGTTGG TTAAGCTCCT ATAGGTAGTG TCTGGGACAG 1020 TGTAGCAGCA GGAGAGCAAA TTCTGGCACC TACCCTTATA AGAATTTATG AACAGTGTTT 1080 TCTGCTAAAA ATAGTAAAGT TCTAGTTCTG CTGACTACAT AACAATGACC AGGGCAAGCA 1140 ACTTGCTTAA TCGCCTCAGT CTCATATATT TTTTTTTCAC TCGTCAGAGG TGGACACTCA 1200 ACTTTCATAA GATAAGTGGC ATGAAAATGC TCTTTGAGCT GTAAAAATAT TGGCTGATTT 1260 ACAAATGACT GTTTTGACGA AGGTATTGGA AAGAACTTTT ATTAGAAGAC AGTGAGTGCT 1320 TCCACAGGCA CTAACCTCTC TGGTGTTTTG AAAATGCTCC AAAGGGCAAA TTCTAGCACT 1380 GTGAAAGATT TGAGAGACGG CTACCTCGTT AGCTGTTCTA TTTCCTCATT ATTATTTTTG 1440 GCATCTCAGA TGGCCACTGA CAGGCATAAA GAGATTATTT CTCCCATATA 1490
|