| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8151174-8151494 | Common:3; Rare:81 | ||||
| chr17:8152352-8152548 | Common:2; Rare:44 | ||||
| chr17:8162890-8163062 | Rare:54 | ||||
| chr17:8176313-8176449 | Rare:47 | ||||
| chr17:8248034-8248136 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8295352-8295518 | Common:1; Rare:45 | ||||
| chr17:8376603-8376781 | Common:1; Rare:75 | ||||
| chr17:8965673-8965802 | Common:1; Rare:37 | ||||
| chr17:10036716-10037074 | Common:4; Rare:59 | ||||
| chr17:10697494-10697660 | Common:4; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:10729453-10729818 | Common:6; Rare:124 | ||||
| chr17:10729972-10730128 | Common:3; Rare:34 | ||||
| chr17:11997444-11997618 | Common:3; Rare:60 | ||||
| chr17:12665742-12666200 | Common:4; Rare:108 | ||||
| chr17:13017618-13017713 | Rare:41; Clinvar (benign):1 |