| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5420054-5420225 | Rare:68 | ||||
| chr17:5486165-5486604 | Common:5; Rare:147 | ||||
| chr17:5486789-5486902 | Common:4; Rare:34 | ||||
| chr17:6640640-6641085 | Common:7; Rare:136 | ||||
| chr17:6651553-6651732 | Common:1; Rare:64 | ||||
| chr17:7012315-7012724 | Rare:134 | ||||
| chr17:7219725-7219964 | Common:3; Rare:95; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7251963-7252219 | Rare:100 | ||||
| chr17:7262453-7262649 | Rare:45 | ||||
| chr17:7351619-7351736 | Rare:22 | ||||
| chr17:7352062-7352196 | Rare:44 | ||||
| chr17:7479496-7479713 | Common:1; Rare:38 | ||||
| chr17:7484203-7484372 | Common:1; Rare:68 | ||||
| chr17:7484697-7484834 | Rare:57 | ||||
| chr17:7497852-7498145 | Common:3; Rare:117 |