Tag | Content |
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EnhancerAtlas ID | HS007-04126 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:109982510-109983690 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr12:109983668-109983681 | AGCAGCTGCCCCC | + | 6.03 |
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| 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 |
GH12I109544 | chr12 | 109982612 | 109983475 |
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Enhancer Sequence | GCTACTGGTA ATTACTCAGC TGTGGGAGCT CCTGGTCATC AGCCTTCAAA CACAGAAACT 60 CAGGTATTTT TCCCAGCAGA CCCTGACCAG CCTCTGTATT TCTCCATAAC GCTGGTCGGC 120 TGGGCACAGC GATCTTGGCA ACAGATTTTG CGAAATAAAC TTGGTCAGTG GATCCCAGTC 180 AACAAAATGT TTTTCCATCT GTTACCCACT TCCTCCTGCC TGTGAAGGGG CAGTGCTCTC 240 TCCTTCTTAT AGGTGAGGCT CTGAGAGGTG GAGTGAGTGA CTTGCCCAGG GACTCAAAGC 300 CAGGATATGA GGAACTGGGA TGTAAGCCCA AGCCTTTGAC CAGGAAGGTG ACCTCACTCA 360 CTCACTTGCC TTCCCTGATC GTCAGAGGCC TGGACAGAAG CCTTCTGTCT CCCAGAGGGG 420 CTAGTCCCAC TGACTCTCCT GACCTGCTCC CATCCCACTA GGGACACTGT CCAGGGGAGG 480 GAGCACACCC CATGTGGGGC TTGGTGTGAA GTCTGCTGGG TGGCTTTGTC ACATTGCAGA 540 TGGTGCCAGA TGAGCCGGGC CCCGCCCAGG AAGCCAGACT GCCAGGGAGT TCAGACTCAG 600 CCAACAAACA GACCCACAGG GCCTCCTGTG CCCCAGGCTG GGTGCTGAGT TACAGCCGTG 660 CACACGGTGG ACGTGATCCC TGCCCTACAG AGCTCACTCT CTGGTGGGAA AGAGTCAGAA 720 CTAATTCAAG GAGGAGGTGT ATGGCCACAT CCTGTGATCA GCGTCCCTGG CATCTAGTGC 780 TGTGCTATTC TGATGCCCAC TCAAGTGGGG AAAGCTGAGG TCAGGAGCTG GTCATTCCCA 840 TGCCCAAGGC CCCAGAGTCA GTTAAGTGGC AGAGCCAGGA TTCAAACCCT GGTCTGCCAC 900 ACTCCAGAGC CCTCACTCGG TTTGAGCAGG CAGAAGAGGG GTGGGAGAAC ATTCTAGGCA 960 AAGGGCTCAG CTTGAGCCAA GCCCCAGGGG CTGCTCTGTC CCTTATCTGG AGCCCGCTGC 1020 CTCCACTGCT TGTCCCACTT ACCCTTGCCG GGGATGCTGC AAACTGACAG ACACACCCAT 1080 TTTGCCAGTG AGTTCCCACA GCATTTTAAA GGACTTCTTC AGGACCCTAG AGCCCTGGTC 1140 TCCCCAAGGC TGCAGAGCAG CAGCTGCCCC CCAGGCACAG 1180
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