Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58007216-58007378 | Common:1; Rare:68 | ||||
chr17:58219231-58219391 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr17:58417532-58417658 | Rare:22 | ||||
chr17:58692501-58692663 | Common:2; Rare:89; Clinvar:9; Clinvar (benign):19 | ||||
chr17:59106706-59107009 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155232-59155536 | Common:1; Rare:55 | ||||
chr17:59331491-59331784 | Common:2; Rare:97 | ||||
chr17:59619590-59620014 | Common:3; Rare:151 | ||||
chr17:59707402-59707732 | Common:3; Rare:89; Clinvar (benign):2 | ||||
chr17:59892877-59893173 | Common:1; Rare:88 | ||||
chr17:59964697-59965111 | Common:2; Rare:124 | ||||
chr17:60078872-60078986 | Common:4; Rare:55 | ||||
chr17:60392019-60392331 | Common:2; Rare:78 | ||||
chr17:60526122-60526329 | Rare:83 | ||||
chr17:63550178-63550507 | Common:2; Rare:71 |