| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42107786-42107962 | Rare:63 | ||||
| chr17:42121338-42121423 | Rare:19 | ||||
| chr17:42154910-42155075 | Common:2; Rare:41 | ||||
| chr17:42194427-42194580 | Rare:29 | ||||
| chr17:42388363-42388765 | Rare:118; Clinvar:3 | ||||
| chr17:42422859-42423422 | Common:2; Rare:176; Clinvar:5 | ||||
| chr17:42458738-42458985 | Common:3; Rare:94 | ||||
| chr17:42552767-42552926 | Common:1; Rare:70 | ||||
| chr17:42566947-42567159 | Common:3; Rare:74 | ||||
| chr17:42577651-42577864 | Common:1; Rare:103 | ||||
| chr17:42609231-42609784 | Common:9; Rare:225; Clinvar (benign):2 | ||||
| chr17:42659188-42659454 | Rare:81 | ||||
| chr17:42676948-42677224 | Common:1; Rare:75 | ||||
| chr17:42745019-42745100 | Common:2; Rare:31 | ||||
| chr17:42761058-42761264 | Rare:56 |