| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30064024-30064499 | Common:2; Rare:173; Clinvar (benign):2 | ||||
| chr16:30065268-30065928 | Rare:333 | ||||
| chr16:30075846-30076408 | Common:4; Rare:243 | ||||
| chr16:30091819-30092219 | Common:3; Rare:144; Clinvar (pathogenic):1 | ||||
| chr16:30096112-30096540 | Common:2; Rare:207 | ||||
| chr16:30123103-30123414 | Common:11; Rare:149 | ||||
| chr16:30183496-30183629 | Common:2; Rare:61 | ||||
| chr16:30355210-30355453 | Common:3; Rare:163 | ||||
| chr16:30355809-30355953 | Common:2; Rare:57 | ||||
| chr16:30370173-30371190 | Common:4; Rare:336 | ||||
| chr16:30378730-30379160 | Common:4; Rare:168 | ||||
| chr16:30395017-30396000 | Common:6; Rare:311 | ||||
| chr16:30407480-30407656 | Rare:117 | ||||
| chr16:30445283-30445790 | Rare:279 | ||||
| chr16:30445841-30446056 | Common:1; Rare:109 |