| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699514-15699773 | Common:3; Rare:68 | ||||
| chr17:15944946-15945249 | Common:1; Rare:79 | ||||
| chr17:15999598-16000032 | Common:3; Rare:186; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039671-16039918 | Common:2; Rare:51 | ||||
| chr17:16040440-16040747 | Common:2; Rare:54 | ||||
| chr17:16194187-16194482 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
| chr17:16215371-16215657 | Common:2; Rare:115 | ||||
| chr17:16217152-16217285 | Rare:51; Clinvar:2 | ||||
| chr17:17496377-17496463 | Rare:22 | ||||
| chr17:17591670-17591926 | Common:1; Rare:67 | ||||
| chr17:17816339-17816472 | Rare:41 | ||||
| chr17:17819399-17819589 | Rare:60 | ||||
| chr17:17819795-17819830 | Rare:3 | ||||
| chr17:17820490-17820807 | Common:2; Rare:48 | ||||
| chr17:17823527-17823847 | Common:5; Rare:148 |