| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:33291677-33291715 | Common:1; Rare:11 | ||||
| chr17:33291898-33292122 | Common:1; Rare:88 | ||||
| chr17:33292624-33292790 | Common:2; Rare:41 | ||||
| chr17:33292957-33293029 | Common:2; Rare:17 | ||||
| chr17:33293243-33293419 | Rare:47 | ||||
| chr17:34255129-34255285 | Rare:40 | ||||
| chr17:34961176-34961215 | Rare:11 | ||||
| chr17:34961220-34961642 | Common:5; Rare:176 | ||||
| chr17:34961791-34961864 | Common:1; Rare:23 | ||||
| chr17:34980340-34980637 | Common:4; Rare:87 | ||||
| chr17:34980661-34981275 | Common:4; Rare:162 | ||||
| chr17:35063622-35063861 | Rare:46 | ||||
| chr17:35089216-35089486 | Common:4; Rare:62 | ||||
| chr17:35119700-35119785 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:35119798-35119960 | Rare:53; Clinvar:2; Clinvar (benign):1 |