| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47831448-47831695 | Rare:82 | ||||
| chr17:47895745-47896278 | Common:3; Rare:157 | ||||
| chr17:47941348-47941746 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48047716-48047902 | Common:1; Rare:43 | ||||
| chr17:48048039-48048463 | Common:1; Rare:120 | ||||
| chr17:48048576-48048833 | Common:4; Rare:51 | ||||
| chr17:48101301-48101672 | Common:3; Rare:107 | ||||
| chr17:48107735-48107825 | Rare:27 | ||||
| chr17:48543919-48543988 | Rare:19 | ||||
| chr17:48610504-48610702 | Common:1; Rare:64 | ||||
| chr17:48613449-48613697 | Common:4; Rare:79 | ||||
| chr17:48614538-48614813 | Rare:72 | ||||
| chr17:48625808-48625945 | Rare:46 | ||||
| chr17:48892298-48892905 | Common:14; Rare:173 | ||||
| chr17:48908184-48908505 | Common:4; Rare:88 |