Tag | Content |
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EnhancerAtlas ID | HS176-41524 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:35847850-35848740 |
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 | GTGAGCCTGC TAATGTTACT TAACCCCCAA GTAGACTTTT TACCCCTGAA GTGTCACATC 60 TGGGAATCTT TTCAACTCAT CTCTAGGCTC TTGGCACCAT GTGACATGCA TGTGAGCACT 120 GCAAAAACTC TTAGATGGTT TCAGACTGCT CAGGCCTTGT CAGCAAGGAT ATCACAGAAA 180 GCAAGACAGG CCTTCCTGGC ATCCTGCATT ACTAGGTCAG ACATATGTCT AAATTAGAAA 240 AATCATAGTT CTCATCTGGG AGAAAGCAGG GGCAAATGTG CTGAAACTGA GGGGCCTGGG 300 TCCTCCTGGA GATTCATCCA GAGATGAGGA AGAAGAGTCT GCAACCATGC TGCAGAGAGA 360 GATCTTGGCC CTTTAAGCTG GGTGAGAAGC ATATACCCCA GTTTTGCTTG ATTGGCCCCT 420 TTTTAGGCCT GCCCCCACAG TGCCTCATTC TATTTTTATG TTAGACACTG TTTCTCTTTC 480 GTATTGCCAG ATGCCCTTTC TACTGTGGCT CACCAAATCC TCCAGCAACA GCTGTTCTAC 540 CAGCCCACTC TCGGCTACAT GCAGATCGAA TGTGATTCAT AATTAGTAAG AATACCTAAG 600 TGTGTCAGGA GCCTGAAGCA TGTAGGGAGA GCATATTCAC TCTCTGGACT TGACACAAGT 660 ATCCTGATTG GCTCCAGAGT GTTCAGTGCT AGATGACTCT TCCTTATCTG GATACAGTGG 720 CTGTCAGCCT GAAAAGACCT TCCCTGTAGC AGGAGTACTA GGAGAGCCTC AAGTGCCTGG 780 CACCACATAA AAAGCTCCCG GTTTCTTTCT TTGTTTTTTT TCTTTTTTTT TTTTTTTTTG 840 AGACAGAGTC TTGCTGTGTT GCCCAGGCTG GAGTGCAGTG GCGCGATCTT 890
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