Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:17281182-17281348 | Rare:69 | ||||
chr17:17591589-17591939 | Common:2; Rare:100 | ||||
chr17:17972578-17972925 | Common:2; Rare:90 | ||||
chr17:18039091-18039422 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18087851-18088009 | Rare:49 | ||||
chr17:18183713-18183931 | Rare:101 | ||||
chr17:18314921-18315319 | Common:1; Rare:112 | ||||
chr17:18781118-18781311 | Common:3; Rare:52 | ||||
chr17:18856189-18856368 | Common:1; Rare:30 | ||||
chr17:18857926-18858221 | Common:6; Rare:74 | ||||
chr17:19362549-19362773 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
chr17:19377514-19377773 | Common:2; Rare:61 | ||||
chr17:19377887-19378031 | Common:1; Rare:36 | ||||
chr17:19378130-19378538 | Common:2; Rare:101 | ||||
chr17:19533774-19533916 | Common:3; Rare:48 |