| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170936-43171296 | Common:2; Rare:229 | ||||
| chr17:43211713-43212094 | Common:6; Rare:139 | ||||
| chr17:43398856-43399019 | Common:2; Rare:84 | ||||
| chr17:43483651-43484044 | Rare:206 | ||||
| chr17:43530749-43531100 | Common:2; Rare:138 | ||||
| chr17:43545827-43546153 | Common:3; Rare:68 | ||||
| chr17:43546252-43546627 | Common:4; Rare:178 | ||||
| chr17:43778887-43779078 | Rare:76 | ||||
| chr17:44004350-44004680 | Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44013950-44014610 | Common:2; Rare:225 | ||||
| chr17:44066108-44066508 | Common:2; Rare:179 | ||||
| chr17:44070612-44070984 | Common:6; Rare:251; Clinvar:8; Clinvar (benign):4 | ||||
| chr17:44093210-44093654 | Common:4; Rare:287 | ||||
| chr17:44111174-44111476 | Rare:159 | ||||
| chr17:44123572-44123864 | Common:6; Rare:163 |