| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47530951-47531296 | Common:1; Rare:94 | ||||
| chr17:47649630-47649980 | Common:1; Rare:134 | ||||
| chr17:47693750-47694091 | Common:1; Rare:58 | ||||
| chr17:47694434-47694632 | Common:5; Rare:57 | ||||
| chr17:47831503-47831614 | Rare:33 | ||||
| chr17:47841081-47841390 | Rare:69 | ||||
| chr17:47851164-47851458 | Common:2; Rare:54 | ||||
| chr17:47896120-47896256 | Rare:38 | ||||
| chr17:47941350-47941712 | Rare:98; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970723-47971148 | Common:4; Rare:103 | ||||
| chr17:48037717-48037862 | Common:2; Rare:40 | ||||
| chr17:48048061-48048400 | Rare:90 | ||||
| chr17:48048643-48048813 | Common:3; Rare:23 | ||||
| chr17:48100818-48101631 | Common:4; Rare:212 | ||||
| chr17:48107427-48107764 | Common:5; Rare:78 |