| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1651249-1651508 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1661722-1662035 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:1684782-1685038 | Common:2; Rare:86; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:1829804-1830096 | Common:7; Rare:123 | ||||
| chr17:2303466-2303633 | Rare:61 | ||||
| chr17:2303770-2303980 | Common:2; Rare:78 | ||||
| chr17:2336423-2336507 | Rare:29 | ||||
| chr17:2511796-2512021 | Common:2; Rare:71 | ||||
| chr17:2593861-2593987 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:3636215-3636500 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr17:3668538-3668828 | Common:3; Rare:115 | ||||
| chr17:3723802-3723932 | Rare:75 | ||||
| chr17:4143020-4143244 | Rare:69 | ||||
| chr17:4143609-4143702 | Common:3; Rare:49 | ||||
| chr17:4263943-4264090 | Rare:58 |