Tag | Content |
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EnhancerAtlas ID | HS141-05338 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr13:76081350-76082730 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr13:76082656-76082667 | GACAGCTGCTG | + | 6.14 | NFYB | MA0502.1 | chr13:76082003-76082018 | CTGATTGGCTCATGG | - | 6.71 | Tcf12 | MA0521.1 | chr13:76082656-76082667 | GACAGCTGCTG | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 76081447 | 76081497 | chr13 | 76082140 | 76082255 |
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Enhancer Sequence | CCACACCTGC CCAGGGTGAG CCAGGCGTGG AGCAGCAAGG GGTGTGTGGG TGAGCAAATG 60 CAGGGTCCAG CCACTGCACA CAGCCAGGCA TGCCAGCTGC TGTGTTGGGG CAGGCAGCTC 120 CAGATGCTGG CACAGGTGCT GGCTCCAAGC AAGGCTGCAG TTGGGCCAGA TACACTGCAC 180 ACAGTTTCTG CTGTGGGCAC CCGCATCTGG ACAAGGGGGA TGTGGTGGCA TCCAGAAGCT 240 TGGAGACAGC AGGGACTGCA GAGACCCAAA GAGGGTGTCA CAGCTCTGGC TTGGTGAGCC 300 CCTAGGTCTG GGATCCCGGA AGGGCCACAG CTCTTCTCTC CTTGTCTCCT TCTCATCACC 360 CACAATGTGG CAAGCGGTGG GGGCTGGGGG GTGTGTTTCA GCCCTGTTTA TGTTATAACT 420 CTTTCAGTCC CACTATTCAG TGAGTCTCAA GTTCTTTTCC CAAGTCCAGG AAGAATGAGG 480 TATGGGGACA GCTGTAGGGT GAGCAAGGTG GAGAGGAGCT TCATTGAGCA ACAGAACAGC 540 TCCCAGGAGA CCTAAAGTGG GTAGTTCCTT CTGGCAGTTG GTAGTCCTGA TGTCTGTGTG 600 AGTCTGGCTG AGTCTCTGGG GTTTTTATGG GTTCCGAAGA GAGGAAGTGC ATACTGATTG 660 GCTCATGGGC GGCCACGGGC AGGCTGGGAA AAGCACCATA AGTTGTCACT CTGGGCTGCA 720 AACTCCACCC TGAACTAGTA GCCTGGTCCC CCAGGCTTCA GGCCATCCCT GGCTTGAAAG 780 TGGAGTTTCA CTGGGGACCC ACCAATAACC TGTCTGCCTC CTGCCATCAA CATGCCATCC 840 AAGGTGCCCA AGCTGTTCAT GCCAAAGGGT GCCTGCAAGC CTGTGCTGAG CTGCCCTCAG 900 CTCCCCTTCT GGCTTCCCTC TTGCACTCAT TGGCATCCAA AGTCTGGAGG TGGCAGGGGG 960 CTGGCATGTT AGCATAGCCC TGAGTGCATG CACACCCAGC CAGGTAGCAA CAGCACCCAG 1020 GCTTGGCCAC AACTTTGCTC TGCACCAGAG TGGGTGCCGG GAGCAGGGAG AGGCCAAACA 1080 GTGGGAGCAG GCACTTCCAA GCCTGCAGGG GCAGGGGCTT CCCAGGCCCC TGAGAGCACA 1140 GGAATGCCTG GGTCCAGAGC CGTGGCCAGG CGGCTACAGC TGTATCCAGG AGCACAGGCC 1200 TCCAGTCTTG CCAACTTGGT AGGGGTAGGG CTCCTGCCCC CTACAGAGGT GCAACCCCAG 1260 CTGCACCTCC CACGCTGCAG CCAGCATCTT CGCAGCGGCC ACTCCAGACA GCTGCTGCTG 1320 CCATCATTGG GACACTGGCA AAAACTGAAT AAGAATTGAA GATTAGGTGA CATCAGTGTT 1380
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