| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2711763-2712033 | Common:2; Rare:76 | ||||
| chr17:3528947-3529106 | Rare:54; Clinvar (benign):1 | ||||
| chr17:3529982-3530382 | Common:5; Rare:167; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:3535420-3535820 | Rare:178 | ||||
| chr17:3636211-3636519 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr17:3668395-3668876 | Common:3; Rare:195 | ||||
| chr17:3723750-3724125 | Common:1; Rare:193 | ||||
| chr17:3845882-3846045 | Rare:43 | ||||
| chr17:3846185-3846465 | Common:1; Rare:91 | ||||
| chr17:3892950-3893500 | Common:5; Rare:157 | ||||
| chr17:4075546-4075946 | Common:2; Rare:148 | ||||
| chr17:4142954-4143237 | Common:3; Rare:99 | ||||
| chr17:4143597-4143798 | Common:5; Rare:118 | ||||
| chr17:4144055-4144186 | Common:1; Rare:44 | ||||
| chr17:4263893-4264096 | Rare:87 |