| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51166702-51166954 | Rare:77 | ||||
| chr17:51260322-51260593 | Common:3; Rare:115 | ||||
| chr17:54968292-54968340 | Rare:19 | ||||
| chr17:54968589-54968798 | Common:3; Rare:97 | ||||
| chr17:56895946-56895989 | Rare:12 | ||||
| chr17:56913395-56913559 | Common:1; Rare:48 | ||||
| chr17:56914005-56914176 | Common:1; Rare:43 | ||||
| chr17:56961012-56961206 | Common:3; Rare:55 | ||||
| chr17:57849979-57850266 | Common:1; Rare:99 | ||||
| chr17:58006341-58006705 | Common:2; Rare:100 | ||||
| chr17:58006963-58007052 | Rare:14 | ||||
| chr17:58007097-58007438 | Common:1; Rare:149 | ||||
| chr17:58083649-58083666 | Rare:3 | ||||
| chr17:58219214-58219372 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58352066-58352481 | Common:6; Rare:146 |