Tag | Content |
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EnhancerAtlas ID | HS098-58716 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:128651190-128652700 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU4F2 | MA0683.1 | chr9:128651968-128651984 | TACATTAATTATGCAG | - | 6.91 | Sox6 | MA0515.1 | chr9:128652529-128652539 | AAAACAATGG | - | 6.02 |
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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 |
GH09I125888 | chr9 | 128650945 | 128653310 |
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Enhancer Sequence | GAATATTCTG GATGATTATG AGTATGAAGT GAAAATGTTT TTCCAAAAAT GTACATTTTT 60 GGGTGTAAAA TATGCTTTGG GAATTTACTC TTTTGACTTT TAGGTATTCT CACCCACAGC 120 AGGTTATGAA AGGGAAAAGT CAGTGACCAC GTATTACAAT AAAATGGCCT TAACGTAATT 180 TGGAAGTGGA TAACAGCCCT ATACACCAGA CACCTTATTG CAAGGCTCTT AGCATCCCCA 240 GGAACGTAGG CCTTAATTTC AGTTAAGTGT GGGTTCGCCC ACATCCCCGT GGTTTCTTGG 300 AATAACTCAC TGACCCGTGG AGAGCTGTCT CCTGGTCCGG GCCTTTCCCT CTCTGGCTGT 360 GGGCTGTTGA AGGGCGTCTG CACACGTGGG GAGCAGGGGC GCTTGCACAC GCACGGGCCG 420 AGCCACGGCT CGCTTGGCAG TGCACACACG CAGCGGCCTC GCCCCTTTCC TCCGGTCCCG 480 AGTTCTGCAT AAAGATGTGT TAGAAATCTC GTTCCTAAAG GATCTAGAAC GATAAATAAT 540 GGATGTATGG GAGCTCGGTT TAAGCTCGAA TTTTCTTTCC TCAGTAGTTT TTGTTCTCAG 600 TCACCTTGAT GAAACAATCT TGAAGCCGCT CCGCTCTCAG TGGCATTTGC AATGAGTCCC 660 TGACAGGCTG ATTTTCCACC CCTGTTGTGA TGCTGCTTTC TCTAGTTAAT ATTCCTGTGT 720 AAGTGTCGCA CAAAAGTAAA CCCAAAGAGC CCGCACATGA CACGGAGGCT GCTCCATTTA 780 CATTAATTAT GCAGTCAGGG CGGTGAGAAT TCGCTGTCAG CCAGCAGGGC GGGGGCGCGC 840 CGCGGCGGGG AGCGGGGCCG GGCCGCGGGG CCTCCCGGCG CGAACGCGGG AGGGGGAGCC 900 GGATCGCCGT CCGCCGCTCC GCGGCTCCGC GCTGCGAGAA CAATGGGCGC GCCCGACGCC 960 CGCCCGCGCT CGCGCTGCCC GGCGCGCCCC GAAAGCCGCG GGGCAGAGCG CCCTGAGCGG 1020 TCCCCCGCGC CGGCGGCCCC GGCTGCGCCC CGCTGTAGCA GCTGACCTTA GCCGGCTGCG 1080 GCCGAGAGAA CGCGCGTTGC CCGCCGACCT TGTGCCCTGG GGTCAGCACC CACTGCAAGT 1140 CAGAACCTCT CCGTGGTCCC AAAGTTAGTG CTTTTCCAAT CCAAACCAGA AACTTGATTT 1200 GAGGCCTGGC GATGGTAGAG GATGCATTTT CTTGATTTCA AACATCTGGG CTGCTGCCGA 1260 CTCCGGTTTC TCAGAGGAGG ACTGCATAAC CACCATGTGA ACATTTTCAA CAGATAGGAA 1320 AAAATTCCCA ACCAGCTTCA AAACAATGGT GGTTGAGAAA AAAATAACTA AGCCTTCACC 1380 ATAAGTATGA AACATCATCT GGGAGGTTTT CCCACGGTAA TTGGCTCTGA AGTATCCTAA 1440 CTTAATGGTT GTGTTTTTCA ACGGGAGACT GAATTCCAAA GGGAATTCCA CAGGGAATTT 1500 AAATGTACAA 1510
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