| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63622126-63622490 | Common:1; Rare:94 | ||||
| chr17:63699284-63699554 | Rare:65 | ||||
| chr17:63699670-63699910 | Common:1; Rare:54 | ||||
| chr17:63700099-63700356 | Common:1; Rare:64 | ||||
| chr17:63741343-63741551 | Rare:35 | ||||
| chr17:63741746-63742114 | Common:3; Rare:132 | ||||
| chr17:63773503-63773868 | Common:2; Rare:119 | ||||
| chr17:63774048-63774212 | Common:2; Rare:58 | ||||
| chr17:63827055-63827508 | Common:5; Rare:131 | ||||
| chr17:63827635-63827758 | Common:1; Rare:24 | ||||
| chr17:63842924-63843212 | Common:2; Rare:62 | ||||
| chr17:64130102-64130402 | Common:7; Rare:75 | ||||
| chr17:64263199-64263456 | Common:2; Rare:92 | ||||
| chr17:64496985-64497194 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:64506244-64506370 | Common:2; Rare:57 |