| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31273636-31273727 | Common:1; Rare:10 | ||||
| chr17:31314003-31314192 | Rare:36 | ||||
| chr17:31321602-31321667 | Rare:9 | ||||
| chr17:32350033-32350209 | Rare:94 | ||||
| chr17:34961456-34961569 | Common:1; Rare:56 | ||||
| chr17:34980409-34980618 | Common:4; Rare:62 | ||||
| chr17:34981146-34981248 | Common:1; Rare:18 | ||||
| chr17:35242910-35243081 | Rare:57 | ||||
| chr17:35578505-35578684 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587184-35587512 | Rare:88 | ||||
| chr17:36210812-36211069 | Rare:27 | ||||
| chr17:36534846-36535020 | Common:3; Rare:80 | ||||
| chr17:36544787-36544976 | Common:3; Rare:62 | ||||
| chr17:37406788-37406924 | Rare:54 | ||||
| chr17:37489709-37489900 | Rare:75 |