| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32342114-32342262 | Rare:44 | ||||
| chr17:32350060-32350204 | Rare:84 | ||||
| chr17:34255135-34255347 | Rare:62 | ||||
| chr17:34961432-34961575 | Common:1; Rare:67 | ||||
| chr17:34980382-34980597 | Common:4; Rare:63 | ||||
| chr17:35089177-35089477 | Common:4; Rare:71 | ||||
| chr17:35242901-35243081 | Rare:59 | ||||
| chr17:35373609-35373851 | Common:4; Rare:47 | ||||
| chr17:35433135-35433461 | Common:5; Rare:74 | ||||
| chr17:35578545-35578684 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr17:35587204-35587530 | Rare:85 | ||||
| chr17:36486476-36486696 | Common:2; Rare:70 | ||||
| chr17:36534787-36535020 | Common:3; Rare:98 | ||||
| chr17:36544794-36545054 | Common:4; Rare:79 | ||||
| chr17:37406814-37406924 | Rare:42 |