| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47693853-47694085 | Common:1; Rare:37 | ||||
| chr17:47831507-47831656 | Rare:40 | ||||
| chr17:47895957-47896278 | Rare:99 | ||||
| chr17:47941328-47941712 | Rare:103; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970740-47971157 | Common:4; Rare:96 | ||||
| chr17:48048039-48048405 | Common:1; Rare:100 | ||||
| chr17:48048602-48048857 | Common:4; Rare:40 | ||||
| chr17:48101266-48101625 | Common:3; Rare:102 | ||||
| chr17:48107427-48107599 | Common:3; Rare:41 | ||||
| chr17:48544587-48544658 | Rare:38 | ||||
| chr17:48544702-48544941 | Common:2; Rare:76 | ||||
| chr17:48610522-48610684 | Rare:50 | ||||
| chr17:48841451-48841791 | Common:2; Rare:49 | ||||
| chr17:48908258-48908407 | Common:2; Rare:34 | ||||
| chr17:48908603-48908744 | Rare:28 |