| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1491120-1491390 | Common:2; Rare:100 | ||||
| chr17:1491606-1491804 | Common:2; Rare:105 | ||||
| chr17:1516561-1516972 | Common:4; Rare:287 | ||||
| chr17:1562693-1562974 | Common:5; Rare:182 | ||||
| chr17:1628250-1628630 | Common:2; Rare:169 | ||||
| chr17:1628793-1629005 | Rare:143 | ||||
| chr17:1629150-1629430 | Rare:83 | ||||
| chr17:1648908-1649239 | Common:6; Rare:217 | ||||
| chr17:1684734-1685072 | Common:4; Rare:197; Clinvar:11; Clinvar (benign):2 | ||||
| chr17:1710310-1710413 | Rare:25 | ||||
| chr17:1716182-1716571 | Common:7; Rare:235 | ||||
| chr17:1724593-1724761 | Common:2; Rare:110 | ||||
| chr17:1829753-1830101 | Common:16; Rare:276 | ||||
| chr17:2029959-2030181 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
| chr17:2303334-2303698 | Rare:216 |