Tag | Content |
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EnhancerAtlas ID | HS184-04915 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:133975540-133976710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr10:133975892-133975904 | TTTATTTTTAGA | - | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I132160 | chr10 | 133974390 | 133977463 |
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Enhancer Sequence | GTTCATGGTG TGGCTCTCGG TCGCTCGGGT GCCCTCAGGT GACCCACAGG CCTGTGAGCA 60 CCGAGGTTTT TTTCTGCACT TCCTGCTCTG CTTCTGGGAG ACACTGGGGC AAGGAGGGGA 120 ATGACTGGTT CCTCCTGGGG CAGTGGTGGC TCTTTATGGC AGGGGCTAGT GCCGACTTTG 180 CCTCTCTGGA CATGGGTGTG GGAGACCGTG GTCTGTGTGG CTGCCGAAGG CAGGGAGGCT 240 CATCCAGGCA GCCCACAGTT CGTGTCACCA CGGAGGTCCT GATGAGCACC TCCCACCACC 300 AGGTGCACGT GAAGCCACCA TGAGGTTAAT TCCAAGCCAG CACTTGACCA GGTTTATTTT 360 TAGAAGCTGG AGCTCATCTT AAAGGCACCA AGCTCTTTTG CTCTAAGAAG TGGAGGTTGA 420 CATGTGAGCT GGTTGTGACT GTAAGAAGTG GAGGTTGATG TGCGAGCTGG TTGTGACAGC 480 TGGGGACAGT TTATTTTGTG GCCGCCAAGA ACAATAAAGT GTAACTGAGG CCCAAAAGCA 540 TTTGTTTCCA TTTCCTAATA TTTCTGCTAT CTCTGAAGAT GTTACATTTG GTTGGGAAGA 600 AAGAGCCTCT GTAGTGTGAG AATTTGTTTT TTACAAAGAT TGTATCAATA AAATTTGCCT 660 AAGAAAAGCT TTGAAATATA CAGAGCAAAC TGCCAAACCC CAGGAATTCA TGAAAAGGTG 720 TGTATTTTGG CTGCTGGGTT ATTATGTATT TTGGCTGCTG GTTATAGCAC CAGGATCGGG 780 TTCCATGGGT CTGTGAATTG GATTTGGGGA GGCAGCGTGT GACCCCACAC TCAGCTCCCT 840 CCCACCTTGC TGTATCCCCA CAGGCCACCT GCAGCCCCTC CACCTCCCAC TCAGCTTCCC 900 CACTTCATAG CTCAGTCCTC CCCCACTCTG GGGTCAGGGT CCTGGCTCTT GCTGGCCTGG 960 TCAGCGTCTC TGCTTCTAGG GTCTTCTCAC AGACTGGGGA GGTCCGTGGG GCCCCTGGTC 1020 CTTCTGCAGA GGCCACAGCA CTGGGTCCCT CCCTGTTGCA TATCCTCTTG GCCCTGCTCC 1080 CAGGCGGAGG GTGGCCCGGC CTCCGTTGCC CTTCCTGAAA GGTTTGTTCT GGGGAGAAGG 1140 CAAGGACTAA GGCGTCTCCC CTTCCGCCCC 1170
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