| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28550592-28550901 | Rare:28 | ||||
| chr17:28567732-28567881 | Rare:20 | ||||
| chr17:28644053-28644168 | Rare:34 | ||||
| chr17:28738025-28738330 | Common:1; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:28738716-28739021 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:28745126-28745320 | Common:1; Rare:48 | ||||
| chr17:28745335-28745639 | Common:2; Rare:73 | ||||
| chr17:28871294-28871469 | Rare:25 | ||||
| chr17:28892934-28893140 | Common:2; Rare:33 | ||||
| chr17:29138663-29138872 | Rare:40 | ||||
| chr17:29139038-29139306 | Common:2; Rare:42 | ||||
| chr17:29141338-29141514 | Common:2; Rare:23 | ||||
| chr17:29145402-29145581 | Common:1; Rare:25 | ||||
| chr17:29148715-29149217 | Common:2; Rare:127 | ||||
| chr17:29149580-29149801 | Rare:31 |