| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:55723014-55723034 | Rare:3 | ||||
| chr17:55731817-55732202 | Common:1; Rare:75 | ||||
| chr17:55750848-55751182 | Common:2; Rare:101 | ||||
| chr17:55751276-55751426 | Common:2; Rare:60 | ||||
| chr17:56833894-56834200 | Common:2; Rare:104 | ||||
| chr17:56913362-56913731 | Common:2; Rare:113 | ||||
| chr17:56913978-56914186 | Common:1; Rare:58 | ||||
| chr17:57084980-57085335 | Rare:119 | ||||
| chr17:57849968-57850274 | Common:1; Rare:107 | ||||
| chr17:57988100-57988512 | Common:6; Rare:118 | ||||
| chr17:58006454-58006686 | Common:1; Rare:71 | ||||
| chr17:58006952-58007355 | Rare:136 | ||||
| chr17:58083208-58083566 | Common:5; Rare:136 | ||||
| chr17:58219216-58219376 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58347205-58347365 | Common:1; Rare:33 |