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EnhancerAtlas ID | HS098-19716 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr15:65341580-65342230 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr15:65341666-65341687 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | RFX1 | MA0509.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | + | 7.18 | RFX1 | MA0509.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | - | 7.18 | RFX2 | MA0600.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | + | 7.55 | RFX2 | MA0600.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | - | 7.56 | RFX5 | MA0510.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | + | 7.66 | RFX5 | MA0510.2 | chr15:65341887-65341903 | AGTTGCTATGGCAACG | - | 7.7 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACACGAAGT AAGGGATTTA TCCAGAGAGC ATGGATTCAA GTTCTTCCCT TGCAAATAAC 60 AGAAACCAAT TCTGCTAACT TGTCCAAAAA AAAAAGAAAA AGAAAAAAAA AGCTCTCGGG 120 GTCGGGGCAG GGGGTGCCCT CTCAGCATCA GGAGCCGGCA GCTGCCTTTC CCTCCGGCAC 180 TTTTCCCTTT TCTCCTCTCT GTGTCGTAGG CGTGCCAATC CCCAGGAGAG AGGCGTGATA 240 GGCCCAGCCT TTGACATGTG GGGAAACACA GGCCTGTGAT TGGCTACCGC ATGACACCCA 300 AGGGACAAGT TGCTATGGCA ACGCGTGGGC GCGCTGTGGG CTCGTAGAAG CCAGGTGCGG 360 ACGCTGAACA GGCAGGCGAA GACCCGAGAT GTCCTTTGCA AGGGTCCCAG AACTCGCCAG 420 TGGCTCAGTC CTCCTCACTC CCAGAACAGT GCTCCTCCAC ACATGCGATG GCTTTTAATA 480 AATATTTGAG TCACTCCCAC TTCCAGTCTC TGCCCCTCCA GGCTCCACGT GCTCCTGGGT 540 TCGTTCGGGT CGTTTTTGTC CCATAACTTT GGGCCAGAGG AGATCTGGAT TTGGGCACAG 600 AGGGAGATCA AACTCGGGTG GGATATCCAG TCATGCTGTC TGCTTTGTTT 650
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