| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47895745-47896280 | Common:3; Rare:158 | ||||
| chr17:47896484-47896584 | Rare:26 | ||||
| chr17:47941350-47941742 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048023-48048443 | Common:1; Rare:118 | ||||
| chr17:48048643-48048862 | Common:3; Rare:33 | ||||
| chr17:48107427-48107796 | Common:5; Rare:86 | ||||
| chr17:48430177-48430302 | Rare:34 | ||||
| chr17:48544475-48544547 | Rare:24 | ||||
| chr17:48544562-48544690 | Rare:68 | ||||
| chr17:48544712-48544835 | Common:2; Rare:38 | ||||
| chr17:48604960-48605133 | Common:1; Rare:30 | ||||
| chr17:48610522-48610772 | Common:1; Rare:91 | ||||
| chr17:48614280-48614310 | Rare:6 | ||||
| chr17:48625848-48625944 | Rare:35 | ||||
| chr17:48892345-48892543 | Common:9; Rare:61 |