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EnhancerAtlas ID | HS034-10112 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr15:65341570-65342230 | 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 | GAAATAGGCC TACACGAAGT AAGGGATTTA TCCAGAGAGC ATGGATTCAA GTTCTTCCCT 60 TGCAAATAAC AGAAACCAAT TCTGCTAACT TGTCCAAAAA AAAAAGAAAA AGAAAAAAAA 120 AGCTCTCGGG GTCGGGGCAG GGGGTGCCCT CTCAGCATCA GGAGCCGGCA GCTGCCTTTC 180 CCTCCGGCAC TTTTCCCTTT TCTCCTCTCT GTGTCGTAGG CGTGCCAATC CCCAGGAGAG 240 AGGCGTGATA GGCCCAGCCT TTGACATGTG GGGAAACACA GGCCTGTGAT TGGCTACCGC 300 ATGACACCCA AGGGACAAGT TGCTATGGCA ACGCGTGGGC GCGCTGTGGG CTCGTAGAAG 360 CCAGGTGCGG ACGCTGAACA GGCAGGCGAA GACCCGAGAT GTCCTTTGCA AGGGTCCCAG 420 AACTCGCCAG TGGCTCAGTC CTCCTCACTC CCAGAACAGT GCTCCTCCAC ACATGCGATG 480 GCTTTTAATA AATATTTGAG TCACTCCCAC TTCCAGTCTC TGCCCCTCCA GGCTCCACGT 540 GCTCCTGGGT TCGTTCGGGT CGTTTTTGTC CCATAACTTT GGGCCAGAGG AGATCTGGAT 600 TTGGGCACAG AGGGAGATCA AACTCGGGTG GGATATCCAG TCATGCTGTC TGCTTTGTTT 660
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