| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40219167-40219494 | Common:3; Rare:114 | ||||
| chr17:40219498-40219694 | Rare:29 | ||||
| chr17:40287549-40287944 | Rare:113 | ||||
| chr17:40309071-40309209 | Rare:44 | ||||
| chr17:40318072-40318291 | Common:1; Rare:47 | ||||
| chr17:40341530-40341930 | Rare:122 | ||||
| chr17:40342027-40342146 | Rare:25 | ||||
| chr17:40351073-40351351 | Common:3; Rare:66 | ||||
| chr17:40417869-40418240 | Rare:117 | ||||
| chr17:40443238-40443470 | Rare:64 | ||||
| chr17:40443710-40444010 | Common:2; Rare:80 | ||||
| chr17:40647756-40648195 | Rare:113 | ||||
| chr17:40818954-40819189 | Common:8; Rare:161; Clinvar (benign):1 | ||||
| chr17:41688573-41688901 | Common:1; Rare:107 | ||||
| chr17:41734615-41734733 | Common:4; Rare:51 |