| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40054296-40054606 | Common:2; Rare:69 | ||||
| chr17:40100584-40100882 | Common:2; Rare:60 | ||||
| chr17:40121816-40122349 | Common:2; Rare:166 | ||||
| chr17:40122522-40122619 | Common:2; Rare:34 | ||||
| chr17:40122907-40123246 | Common:1; Rare:96 | ||||
| chr17:40131386-40131584 | Common:1; Rare:35 | ||||
| chr17:40140177-40140594 | Common:5; Rare:201 | ||||
| chr17:40140625-40140909 | Common:1; Rare:104 | ||||
| chr17:40219152-40219783 | Common:3; Rare:168 | ||||
| chr17:40287817-40288102 | Rare:61; Clinvar:1 | ||||
| chr17:40291296-40291657 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:40309077-40309224 | Rare:46 | ||||
| chr17:40318085-40318293 | Common:1; Rare:46 | ||||
| chr17:40342042-40342176 | Common:1; Rare:24 | ||||
| chr17:40417838-40418199 | Rare:113 |