| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16040439-16040552 | Rare:21 | ||||
| chr17:16058549-16058708 | Common:2; Rare:44 | ||||
| chr17:16080490-16080719 | Common:2; Rare:56 | ||||
| chr17:16215522-16215657 | Common:1; Rare:53 | ||||
| chr17:16381019-16381180 | Common:3; Rare:79 | ||||
| chr17:16448061-16448343 | Common:2; Rare:57 | ||||
| chr17:16972057-16972195 | Rare:33; Clinvar:1 | ||||
| chr17:17042270-17042449 | Common:15; Rare:62 | ||||
| chr17:17476753-17477044 | Common:3; Rare:71 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 | ||||
| chr17:17591643-17591911 | Common:1; Rare:75 | ||||
| chr17:17823552-17823870 | Common:5; Rare:146 | ||||
| chr17:18039102-18039373 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087809-18088026 | Rare:58 | ||||
| chr17:18183756-18183986 | Common:1; Rare:104 |