| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40140141-40140551 | Common:5; Rare:191 | ||||
| chr17:40140569-40140795 | Common:1; Rare:96 | ||||
| chr17:40219178-40219431 | Common:3; Rare:93 | ||||
| chr17:40318030-40318309 | Common:1; Rare:58 | ||||
| chr17:40342038-40342417 | Common:1; Rare:81 | ||||
| chr17:41528279-41528337 | Rare:14 | ||||
| chr17:41688613-41688940 | Common:1; Rare:127 | ||||
| chr17:41812644-41813040 | Common:2; Rare:91; Clinvar:5 | ||||
| chr17:42017383-42017482 | Rare:44 | ||||
| chr17:42422981-42423283 | Common:1; Rare:97; Clinvar:3 | ||||
| chr17:42423311-42423462 | Common:1; Rare:34 | ||||
| chr17:42458806-42458945 | Common:2; Rare:41 | ||||
| chr17:42567009-42567136 | Common:3; Rare:40 | ||||
| chr17:42577671-42577825 | Rare:72 | ||||
| chr17:42609321-42609732 | Common:8; Rare:173; Clinvar (benign):2 |