| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47323864-47323992 | Common:1; Rare:44 | ||||
| chr17:47649498-47649965 | Common:1; Rare:168 | ||||
| chr17:47821757-47821893 | Common:1; Rare:29 | ||||
| chr17:47831503-47831656 | Rare:41 | ||||
| chr17:47941328-47941712 | Rare:103; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970751-47971152 | Common:4; Rare:91 | ||||
| chr17:48048054-48048460 | Rare:115 | ||||
| chr17:48101092-48101598 | Common:3; Rare:138 | ||||
| chr17:48830915-48831056 | Common:3; Rare:40 | ||||
| chr17:48892323-48892656 | Common:10; Rare:101 | ||||
| chr17:48944747-48944909 | Common:2; Rare:59 | ||||
| chr17:49210511-49210711 | Rare:33 | ||||
| chr17:49414828-49415110 | Common:1; Rare:66 | ||||
| chr17:49677945-49678355 | Rare:99 | ||||
| chr17:49707989-49708291 | Rare:113 |