| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35578427-35578788 | Common:6; Rare:196; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:35587145-35587619 | Common:1; Rare:295 | ||||
| chr17:35795510-35796100 | Rare:184 | ||||
| chr17:35808950-35809200 | Common:4; Rare:58 | ||||
| chr17:35809243-35809570 | Common:1; Rare:244 | ||||
| chr17:35930684-35930925 | Rare:145 | ||||
| chr17:36486429-36486743 | Common:9; Rare:276 | ||||
| chr17:36534053-36534453 | Common:1; Rare:193 | ||||
| chr17:36534697-36535145 | Common:9; Rare:404 | ||||
| chr17:36544712-36545091 | Common:14; Rare:258 | ||||
| chr17:36545350-36545695 | Common:6; Rare:312 | ||||
| chr17:36591711-36591956 | Rare:100 | ||||
| chr17:36592410-36592760 | Common:4; Rare:71 | ||||
| chr17:36601311-36601702 | Common:7; Rare:227 | ||||
| chr17:36601703-36602103 | Rare:205 |