| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47530925-47531290 | Common:2; Rare:103 | ||||
| chr17:47649420-47650040 | Common:2; Rare:214 | ||||
| chr17:47650130-47650443 | Rare:109 | ||||
| chr17:47650480-47650842 | Common:4; Rare:138 | ||||
| chr17:47831501-47831620 | Rare:34 | ||||
| chr17:47896459-47896565 | Rare:22 | ||||
| chr17:47941341-47941732 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970759-47971171 | Common:4; Rare:96 | ||||
| chr17:48048023-48048423 | Common:1; Rare:109 | ||||
| chr17:48048592-48048847 | Common:4; Rare:42 | ||||
| chr17:48055790-48055984 | Rare:30 | ||||
| chr17:48100996-48101238 | Rare:64 | ||||
| chr17:48101273-48101533 | Common:3; Rare:73 | ||||
| chr17:48107427-48107817 | Common:5; Rare:94 | ||||
| chr17:48603998-48604250 | Common:2; Rare:64 |