| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60249434-60249615 | Rare:31 | ||||
| chr17:60390993-60391419 | Rare:73 | ||||
| chr17:60435534-60435798 | Rare:44 | ||||
| chr17:60435990-60436108 | Rare:23 | ||||
| chr17:60442246-60442541 | Common:3; Rare:52 | ||||
| chr17:60442872-60442896 | Rare:6 | ||||
| chr17:60442989-60443259 | Common:2; Rare:40 | ||||
| chr17:60524859-60525129 | Common:2; Rare:55 | ||||
| chr17:60599146-60599380 | Common:1; Rare:46 | ||||
| chr17:60599503-60599643 | Rare:29 | ||||
| chr17:60600812-60600840 | Rare:6 | ||||
| chr17:60600850-60600929 | Rare:17; Clinvar (benign):1 | ||||
| chr17:60601244-60601403 | Rare:30 | ||||
| chr17:60602060-60602291 | Rare:40 | ||||
| chr17:60744021-60744162 | Common:1; Rare:22 |