Tag | Content |
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EnhancerAtlas ID | HS116-17367 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:47240450-47241420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr19:47241128-47241140 | TCTATAAATAGC | + | 6.37 | MEF2B | MA0660.1 | chr19:47241128-47241140 | TCTATAAATAGC | + | 6.27 |
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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 |
GH19I046736 | chr19 | 47239777 | 47241489 |
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Enhancer Sequence | GGGTTCAAGC CCAGCTCTGC CCCATCCCAG CTGTGTGACC CTGAGTTAGT GTAAGCCGTG 60 TCAGTTTCGT CCTCTGAGAA ATGAGCTTAA TGATAACAGC ATCTCCCTCT TGGGAGTGCT 120 GAGAGGATGC AATGAGATAA TTTGCTTAGT ATTTTATTCA AGTCTTTCCT GGGCATCTAC 180 GCTGTGCCTG GCCAGGGGCC TGGGCTACAT GGGTAAACAA AGACCTGCCC TTGTGGAACT 240 TCCGTTCTAG TGAGAGGAGC TGGCAGCAGG TAATGACCAT CACTATCAGC TGAGCACACA 300 AGGTCTTCTC AGCTTGCCTC GGCCAAGCTT CCCCCTCACC CAGCCCGCCC TCCCACATCC 360 TCTGCCCTAC ACTGTTTGCC CAGGCACACT GACCGACTCC CTGTCCCCTA ACCCTTTCAG 420 CGTGCGTCTC TGTATCTGTG CTCTCTCCCC TGACTCTCCT GCTGGGGAAC GGAGTCATCT 480 TTCAAGGAGC TTAGACTCTA AGGGACCAGA GGGTAGAGAC CATGTCTCCC GTGCTCTCTG 540 CTGTATTCCT GATCTGTGAT ACAAAGCCTG TACCCTACAA ATAAAGTCTT TTTTGGATGA 600 ACGATTGAAC GGCAACCCTG TTCAAACGCC ACCTCCTCAG TGACGTCTTC CCCGGCTTTC 660 CCGCACCGTC CCCAGCACTC TATAAATAGC CCTGGCGCCC ACTCCTCGCA AAGGGATCCC 720 GTGAGCTGCT CGTGTGTCTG CCTCTGTTGC ACAGGGGGAC CCAAGCGGGA CTGGCCCCCA 780 GGGTCCAGCA CGGGACCTGG CAGCCCATAG GGAGGGCTCT GAGAGTGAGA TTCCGCCCCT 840 CCCCAGCCCC GGGGCCGATT CTGCCTTCTA AGGAGCAAAG TGAGAAAGAG GCACCCCATC 900 TTCCTGCTTC TCCAGAACAC TCAGCTTCTG CGGGAGGGTG CCGACAGTGC GAGCATCAGA 960 GGGTGGGTAC 970
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