| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46922869-46923174 | Common:2; Rare:79; Clinvar (benign):6 | ||||
| chr17:47189181-47189538 | Common:1; Rare:98 | ||||
| chr17:47323894-47323962 | Rare:21 | ||||
| chr17:47649614-47649936 | Common:1; Rare:123 | ||||
| chr17:47650076-47650271 | Rare:55 | ||||
| chr17:47831507-47831614 | Rare:32 | ||||
| chr17:47895940-47896253 | Rare:94 | ||||
| chr17:47941345-47941712 | Rare:99; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970762-47971145 | Common:4; Rare:86 | ||||
| chr17:48048061-48048400 | Rare:90 | ||||
| chr17:48101086-48101533 | Common:3; Rare:119 | ||||
| chr17:48944740-48944864 | Common:1; Rare:48 | ||||
| chr17:49230768-49230887 | Common:2; Rare:28 | ||||
| chr17:49414833-49415120 | Common:1; Rare:68 | ||||
| chr17:49708132-49708303 | Rare:58 |