| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30064333-30064493 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr16:30065434-30065725 | Rare:82 | ||||
| chr16:30069495-30070022 | Common:1; Rare:197; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075874-30076059 | Common:1; Rare:62 | ||||
| chr16:30123048-30123381 | Common:6; Rare:99 | ||||
| chr16:30123475-30123626 | Rare:23 | ||||
| chr16:30193654-30193913 | |||||
| chr16:30355211-30355527 | Common:2; Rare:101 | ||||
| chr16:30355849-30355942 | Rare:21 | ||||
| chr16:30407480-30407637 | Rare:52 | ||||
| chr16:30534554-30534636 | Common:1; Rare:29 | ||||
| chr16:30534871-30535102 | Common:3; Rare:77 | ||||
| chr16:30558496-30558669 | Common:1; Rare:52 | ||||
| chr16:30571558-30571738 | Rare:52 | ||||
| chr16:30585583-30585902 | Common:1; Rare:66 |