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EnhancerAtlas ID | HS017-11072 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr15:65341430-65342230 | 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 | ATTTCTTTTT GTTTTGTAAA GTATGGATGC TAGAAAATTT TATATTAAGT AGTAATAATG 60 CAGTTAGTAC AAGAAGACGT CAAAATGTCT GACTGTTTTG AGATTGACTG AGGTTCAGTT 120 TATTATTAAT AGTTGGGATG GAAATAGGCC TACACGAAGT AAGGGATTTA TCCAGAGAGC 180 ATGGATTCAA GTTCTTCCCT TGCAAATAAC AGAAACCAAT TCTGCTAACT TGTCCAAAAA 240 AAAAAGAAAA AGAAAAAAAA AGCTCTCGGG GTCGGGGCAG GGGGTGCCCT CTCAGCATCA 300 GGAGCCGGCA GCTGCCTTTC CCTCCGGCAC TTTTCCCTTT TCTCCTCTCT GTGTCGTAGG 360 CGTGCCAATC CCCAGGAGAG AGGCGTGATA GGCCCAGCCT TTGACATGTG GGGAAACACA 420 GGCCTGTGAT TGGCTACCGC ATGACACCCA AGGGACAAGT TGCTATGGCA ACGCGTGGGC 480 GCGCTGTGGG CTCGTAGAAG CCAGGTGCGG ACGCTGAACA GGCAGGCGAA GACCCGAGAT 540 GTCCTTTGCA AGGGTCCCAG AACTCGCCAG TGGCTCAGTC CTCCTCACTC CCAGAACAGT 600 GCTCCTCCAC ACATGCGATG GCTTTTAATA AATATTTGAG TCACTCCCAC TTCCAGTCTC 660 TGCCCCTCCA GGCTCCACGT GCTCCTGGGT TCGTTCGGGT CGTTTTTGTC CCATAACTTT 720 GGGCCAGAGG AGATCTGGAT TTGGGCACAG AGGGAGATCA AACTCGGGTG GGATATCCAG 780 TCATGCTGTC TGCTTTGTTT 800
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