Tag | Content |
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EnhancerAtlas ID | HS116-34479 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:35847870-35848670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr9:35848376-35848386 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr9:35848376-35848386 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr9:35848376-35848386 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr9:35848376-35848386 | AACAGCTGTT | - | 6.02 | NEUROG1 | MA0623.2 | chr9:35848069-35848079 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr9:35848069-35848079 | GACATATGTC | - | 6.02 | SOX10 | MA0442.2 | chr9:35848656-35848667 | TTCTTTGTTTT | - | 6.62 |
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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 |
GH09I035847 | chr9 | 35847359 | 35849309 |
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Enhancer Sequence | TAACCCCCAA GTAGACTTTT TACCCCTGAA GTGTCACATC TGGGAATCTT TTCAACTCAT 60 CTCTAGGCTC TTGGCACCAT GTGACATGCA TGTGAGCACT GCAAAAACTC TTAGATGGTT 120 TCAGACTGCT CAGGCCTTGT CAGCAAGGAT ATCACAGAAA GCAAGACAGG CCTTCCTGGC 180 ATCCTGCATT ACTAGGTCAG ACATATGTCT AAATTAGAAA AATCATAGTT CTCATCTGGG 240 AGAAAGCAGG GGCAAATGTG CTGAAACTGA GGGGCCTGGG TCCTCCTGGA GATTCATCCA 300 GAGATGAGGA AGAAGAGTCT GCAACCATGC TGCAGAGAGA GATCTTGGCC CTTTAAGCTG 360 GGTGAGAAGC ATATACCCCA GTTTTGCTTG ATTGGCCCCT TTTTAGGCCT GCCCCCACAG 420 TGCCTCATTC TATTTTTATG TTAGACACTG TTTCTCTTTC GTATTGCCAG ATGCCCTTTC 480 TACTGTGGCT CACCAAATCC TCCAGCAACA GCTGTTCTAC CAGCCCACTC TCGGCTACAT 540 GCAGATCGAA TGTGATTCAT AATTAGTAAG AATACCTAAG TGTGTCAGGA GCCTGAAGCA 600 TGTAGGGAGA GCATATTCAC TCTCTGGACT TGACACAAGT ATCCTGATTG GCTCCAGAGT 660 GTTCAGTGCT AGATGACTCT TCCTTATCTG GATACAGTGG CTGTCAGCCT GAAAAGACCT 720 TCCCTGTAGC AGGAGTACTA GGAGAGCCTC AAGTGCCTGG CACCACATAA AAAGCTCCCG 780 GTTTCTTTCT TTGTTTTTTT 800
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