| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941251-47941819 | Rare:148; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr17:47970689-47971211 | Common:4; Rare:136 | ||||
| chr17:48037087-48037236 | Rare:50 | ||||
| chr17:48047719-48047922 | Common:1; Rare:44 | ||||
| chr17:48047999-48048435 | Common:1; Rare:126 | ||||
| chr17:48048557-48048881 | Common:4; Rare:68 | ||||
| chr17:48049205-48049294 | Rare:26 | ||||
| chr17:48101087-48101200 | Rare:33 | ||||
| chr17:48101334-48101675 | Common:2; Rare:100 | ||||
| chr17:48101831-48101898 | Rare:12 | ||||
| chr17:48107337-48107640 | Common:4; Rare:72 | ||||
| chr17:48107713-48107977 | Common:2; Rare:62 | ||||
| chr17:48111728-48111978 | Common:2; Rare:41 | ||||
| chr17:48430033-48430398 | Common:1; Rare:101 | ||||
| chr17:48543203-48543372 | Common:3; Rare:95 |