| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40140715-40140787 | Rare:31 | ||||
| chr17:40219184-40219476 | Common:3; Rare:104 | ||||
| chr17:40318079-40318308 | Common:1; Rare:49 | ||||
| chr17:40342026-40342433 | Common:1; Rare:87 | ||||
| chr17:40501610-40501740 | Rare:31 | ||||
| chr17:40885220-40885244 | Rare:3 | ||||
| chr17:41527811-41528396 | Common:4; Rare:193; Clinvar:4 | ||||
| chr17:41688635-41689069 | Common:3; Rare:172 | ||||
| chr17:41785680-41785735 | Rare:9 | ||||
| chr17:41785957-41786222 | Common:1; Rare:52 | ||||
| chr17:41786669-41786849 | Common:2; Rare:51 | ||||
| chr17:41812602-41813254 | Common:3; Rare:163; Clinvar:9 | ||||
| chr17:41820702-41821002 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:41836189-41836329 | Rare:40 | ||||
| chr17:41918941-41919072 | Rare:63 |