| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30007683-30007868 | Rare:42 | ||||
| chr16:30021283-30021487 | Rare:38 | ||||
| chr16:30052940-30053216 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr16:30053471-30053525 | Rare:17; Clinvar (benign):1 | ||||
| chr16:30064096-30064247 | Rare:32 | ||||
| chr16:30064327-30064444 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr16:30064706-30064806 | Rare:17 | ||||
| chr16:30064967-30065917 | Rare:283 | ||||
| chr16:30066031-30066137 | Rare:32 | ||||
| chr16:30066449-30066799 | Rare:90 | ||||
| chr16:30066946-30067215 | Common:1; Rare:71 | ||||
| chr16:30067303-30067476 | Common:1; Rare:46; Clinvar:5 | ||||
| chr16:30075830-30076083 | Common:1; Rare:85 | ||||
| chr16:30076424-30076585 | Rare:47 | ||||
| chr16:30091873-30092161 | Common:1; Rare:65 |