| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46193411-46193612 | Common:3; Rare:55 | ||||
| chr17:46225353-46225496 | Common:2; Rare:41 | ||||
| chr17:46922878-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189242-47189568 | Rare:83 | ||||
| chr17:47323734-47323776 | Rare:15 | ||||
| chr17:47323868-47324009 | Common:1; Rare:50 | ||||
| chr17:47530924-47531294 | Common:2; Rare:104 | ||||
| chr17:47649543-47649969 | Common:1; Rare:157 | ||||
| chr17:47679865-47680133 | Common:1; Rare:49 | ||||
| chr17:47820274-47820563 | Rare:62 | ||||
| chr17:47831507-47831616 | Rare:32 | ||||
| chr17:47895928-47896271 | Rare:107 | ||||
| chr17:47941356-47941708 | Rare:95; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47957650-47957675 | Rare:2 | ||||
| chr17:47957678-47958041 | Common:2; Rare:60 |