| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45316969-45317401 | Common:6; Rare:115 | ||||
| chr17:46045633-46045673 | Rare:9 | ||||
| chr17:46192825-46193200 | Common:4; Rare:98 | ||||
| chr17:46193411-46193605 | Common:3; Rare:54 | ||||
| chr17:46923013-46923245 | Common:3; Rare:95; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:47189186-47189591 | Common:1; Rare:109 | ||||
| chr17:47323853-47324026 | Common:2; Rare:66 | ||||
| chr17:47530880-47531216 | Common:2; Rare:87 | ||||
| chr17:47649397-47650073 | Common:2; Rare:234 | ||||
| chr17:47650115-47650439 | Rare:113 | ||||
| chr17:47650487-47650820 | Common:3; Rare:124 | ||||
| chr17:47651268-47651477 | Rare:44 | ||||
| chr17:47669681-47670146 | Common:1; Rare:66 | ||||
| chr17:47676404-47676726 | Rare:62 | ||||
| chr17:47693787-47694174 | Common:1; Rare:59 |