| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35809261-35809601 | Rare:142 | ||||
| chr17:35809720-35809947 | Common:2; Rare:74 | ||||
| chr17:35809956-35809978 | Rare:8 | ||||
| chr17:35930090-35930331 | Common:2; Rare:74 | ||||
| chr17:35930698-35930977 | Common:1; Rare:77 | ||||
| chr17:36486442-36486764 | Common:3; Rare:118 | ||||
| chr17:36486915-36486998 | Rare:36; Clinvar (pathogenic):1 | ||||
| chr17:36534157-36534406 | Rare:66 | ||||
| chr17:36534697-36534751 | Rare:13 | ||||
| chr17:36534761-36535118 | Common:3; Rare:138 | ||||
| chr17:36535229-36535263 | Common:3; Rare:12 | ||||
| chr17:36535310-36535618 | Common:2; Rare:95 | ||||
| chr17:36544036-36544394 | Common:2; Rare:67 | ||||
| chr17:36544707-36545094 | Common:6; Rare:110 | ||||
| chr17:36545111-36545246 | Rare:30 |