| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30906205-30906349 | Common:1; Rare:40 | ||||
| chr17:31297168-31297343 | Rare:29 | ||||
| chr17:31901653-31901893 | Common:2; Rare:78 | ||||
| chr17:32142327-32142690 | Common:8; Rare:148 | ||||
| chr17:32342143-32342262 | Rare:24 | ||||
| chr17:32350002-32350198 | Rare:101 | ||||
| chr17:32486450-32486714 | Common:1; Rare:98 | ||||
| chr17:34961489-34961585 | Common:1; Rare:49 | ||||
| chr17:34962034-34962241 | Rare:77 | ||||
| chr17:35242910-35243081 | Rare:57 | ||||
| chr17:35578498-35578746 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587222-35587579 | Rare:87 | ||||
| chr17:36196748-36196859 | Common:1; Rare:9 | ||||
| chr17:36486528-36486702 | Common:2; Rare:64 | ||||
| chr17:36534830-36535033 | Common:3; Rare:94 |