| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19377851-19378028 | Common:2; Rare:47 | ||||
| chr17:19378132-19378554 | Common:2; Rare:100 | ||||
| chr17:19387169-19387369 | Rare:47 | ||||
| chr17:19648602-19648967 | Common:3; Rare:124 | ||||
| chr17:19977796-19978178 | Common:2; Rare:104 | ||||
| chr17:21043389-21043531 | Common:1; Rare:54 | ||||
| chr17:21214118-21214353 | Common:2; Rare:109 | ||||
| chr17:27293975-27294116 | Common:1; Rare:56 | ||||
| chr17:27560237-27560338 | Common:1; Rare:24 | ||||
| chr17:27577250-27577470 | Common:2; Rare:43 | ||||
| chr17:28318920-28319251 | Common:3; Rare:115 | ||||
| chr17:28335376-28335820 | Common:1; Rare:106 | ||||
| chr17:28357451-28357699 | Common:5; Rare:126; Clinvar (pathogenic):1 | ||||
| chr17:28598970-28599115 | Common:1; Rare:48 | ||||
| chr17:28645106-28645271 | Common:1; Rare:62 |