| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4939916-4940285 | Common:2; Rare:112 | ||||
| chr17:4948932-4949135 | Common:1; Rare:66 | ||||
| chr17:4987640-4987753 | Rare:47 | ||||
| chr17:5191843-5192007 | Rare:51 | ||||
| chr17:5419639-5419882 | Common:3; Rare:73 | ||||
| chr17:5420122-5420225 | Rare:42 | ||||
| chr17:5486149-5486511 | Common:4; Rare:133 | ||||
| chr17:5584445-5584599 | Common:1; Rare:32 | ||||
| chr17:6640651-6641085 | Common:7; Rare:133 | ||||
| chr17:7012315-7012745 | Rare:139 | ||||
| chr17:7251978-7252311 | Common:1; Rare:125 | ||||
| chr17:7479517-7479740 | Common:1; Rare:39 | ||||
| chr17:7484215-7484391 | Common:2; Rare:77 | ||||
| chr17:7561796-7562005 | Common:2; Rare:55 | ||||
| chr17:7583547-7583886 | Common:1; Rare:138; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |