| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1684419-1684515 | Rare:42 | ||||
| chr17:1684729-1685080 | Common:2; Rare:122; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1710296-1710533 | Rare:61 | ||||
| chr17:1716126-1716912 | Common:5; Rare:232 | ||||
| chr17:1716993-1717391 | Common:1; Rare:81 | ||||
| chr17:1724407-1724795 | Common:5; Rare:115 | ||||
| chr17:1725109-1725264 | Rare:53 | ||||
| chr17:1761890-1762082 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1763056-1763337 | Rare:59 | ||||
| chr17:1829746-1830106 | Common:9; Rare:148 | ||||
| chr17:2025332-2025512 | Rare:55 | ||||
| chr17:2029917-2030231 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
| chr17:2030661-2030822 | Rare:32 | ||||
| chr17:2041898-2042165 | Common:4; Rare:117 | ||||
| chr17:2054133-2054154 | Rare:5 |