Tag | Content |
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EnhancerAtlas ID | HS060-13890 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:1939390-1939820 |
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) |
RFX1 | MA0509.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | + | 6.08 | RFX1 | MA0509.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | - | 6.15 | RFX2 | MA0600.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | - | 6.75 | RFX2 | MA0600.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | + | 6.85 | RFX5 | MA0510.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | - | 7.43 | RFX5 | MA0510.2 | chr17:1939558-1939574 | GGTTGCCTTGGCAACG | + | 7.51 |
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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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Enhancer Sequence | GTGGGGCCAG GACACCTGGA CGGTGGCGGG GCTGGCAGGG AGGCAGGCTG CACATTCATC 60 TTCCCCATGG CAGTGCCTTC TTGTCCTGCT TGGAGACACA AGGTCCCTCC TGGTTTCTGG 120 GGTGGCCTCT GCCTTCCCGC TCTGCAGGTA GATCTTTCCT TTGGATTTGG TTGCCTTGGC 180 AACGGTGCTC TGTCCCAGAT GCAGGTGTTT GAAAGGCTGT TGGTTGTAGA GCAGGCTGGG 240 CCCCGGCCGG GTGACAGAGA AGTCTGATTG AGAAGGAGCT TCTAGGGGAT CTGTGACCCC 300 CCTCTTCTCC TACCCTGTCC TTTTACCCCC AGGCTGAAGC CACTGCGCCT GGCTGCTCAG 360 AGACCTGAGC CTGGCCGGGC CCTCTGCTGC TCCTGCCTTC CCAAACAGCC CCTGAACTCC 420 TCCCTCCCAC 430
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