| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21599356-21599676 | Common:8; Rare:221 | ||||
| chr16:21599660-21600200 | Common:1; Rare:257 | ||||
| chr16:21952973-21953413 | Common:2; Rare:217; Clinvar (benign):6 | ||||
| chr16:22007820-22008260 | Rare:163 | ||||
| chr16:22205993-22206359 | Common:2; Rare:192 | ||||
| chr16:22297419-22297881 | Common:6; Rare:219 | ||||
| chr16:22374575-22374864 | Common:1; Rare:98 | ||||
| chr16:22436910-22437103 | Rare:111 | ||||
| chr16:22437120-22437440 | Rare:151 | ||||
| chr16:22437446-22437730 | Common:3; Rare:112 | ||||
| chr16:23148580-23149060 | Common:4; Rare:282 | ||||
| chr16:23149358-23149810 | Common:6; Rare:251 | ||||
| chr16:23452463-23452812 | Rare:88; Clinvar (benign):1 | ||||
| chr16:23453114-23453232 | Rare:37 | ||||
| chr16:23453140-23453258 | Rare:37 |