| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53130987-53131128 | Common:2; Rare:42 | ||||
| chr16:53131205-53131329 | Rare:41 | ||||
| chr16:53131437-53131603 | Common:4; Rare:46 | ||||
| chr16:53207867-53208042 | Rare:27 | ||||
| chr16:53208305-53208596 | Rare:54 | ||||
| chr16:53433717-53433983 | Common:4; Rare:37 | ||||
| chr16:53434367-53434644 | Common:1; Rare:107 | ||||
| chr16:53434652-53435009 | Common:3; Rare:120 | ||||
| chr16:53435040-53435195 | Common:1; Rare:35 | ||||
| chr16:53435213-53435653 | Common:2; Rare:98 | ||||
| chr16:53502914-53503088 | Rare:56 | ||||
| chr16:53503150-53503804 | Common:10; Rare:192 | ||||
| chr16:53504199-53504362 | Common:1; Rare:30 | ||||
| chr16:53703778-53704329 | Common:1; Rare:166; Clinvar:6; Clinvar (benign):2 | ||||
| chr16:54285462-54285574 | Rare:41 |