| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2041864-2042156 | Common:6; Rare:140 | ||||
| chr17:2172565-2172965 | Rare:185 | ||||
| chr17:2303440-2303656 | Rare:78 | ||||
| chr17:2303695-2304025 | Common:2; Rare:123 | ||||
| chr17:2336441-2336651 | Rare:73 | ||||
| chr17:2337313-2337535 | Rare:65 | ||||
| chr17:2392610-2393050 | Common:8; Rare:195 | ||||
| chr17:2393750-2394050 | Common:3; Rare:120 | ||||
| chr17:2396720-2397110 | Common:2; Rare:94 | ||||
| chr17:2401027-2401337 | Rare:100 | ||||
| chr17:2401350-2401780 | Common:2; Rare:133 | ||||
| chr17:2511779-2512031 | Common:2; Rare:74 | ||||
| chr17:2593024-2593275 | Rare:54 | ||||
| chr17:2593457-2593733 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2594083-2594209 | Rare:38 |