| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46192729-46193270 | Common:13; Rare:216; Clinvar (benign):6 | ||||
| chr17:46193295-46193605 | Common:9; Rare:149 | ||||
| chr17:46193986-46194241 | Common:5; Rare:43 | ||||
| chr17:46225213-46225613 | Common:6; Rare:132 | ||||
| chr17:46922816-46923193 | Common:8; Rare:208; Clinvar:3; Clinvar (benign):14 | ||||
| chr17:47189174-47189577 | Common:2; Rare:208 | ||||
| chr17:47323610-47324180 | Common:9; Rare:262 | ||||
| chr17:47530958-47531217 | Common:1; Rare:126 | ||||
| chr17:47649292-47650287 | Common:3; Rare:567 | ||||
| chr17:47650410-47650870 | Common:7; Rare:302 | ||||
| chr17:47821687-47822170 | Common:5; Rare:121 | ||||
| chr17:47831460-47831689 | Rare:129 | ||||
| chr17:47841183-47841445 | Rare:94 | ||||
| chr17:47895552-47896625 | Common:14; Rare:500 | ||||
| chr17:47941268-47941761 | Rare:236; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):2 |