| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:369800-370270 | Common:9; Rare:234; Clinvar (benign):1 | ||||
| chr16:370428-370830 | Common:31; Rare:276 | ||||
| chr16:370908-371316 | Common:3; Rare:186 | ||||
| chr16:381802-382207 | Common:35; Rare:532 | ||||
| chr16:396310-396972 | Common:23; Rare:517 | ||||
| chr16:397104-397328 | Common:16; Rare:252 | ||||
| chr16:397490-397777 | Common:3; Rare:31 | ||||
| chr16:397814-398305 | Common:10; Rare:318 | ||||
| chr16:398494-398894 | Common:1; Rare:96 | ||||
| chr16:401617-402108 | Common:15; Rare:1111 | ||||
| chr16:405620-406220 | Common:4; Rare:140 | ||||
| chr16:424704-425465 | Common:2; Rare:184 | ||||
| chr16:425370-425770 | Common:7; Rare:540 | ||||
| chr16:527227-528866 | Common:20; Rare:1348 | ||||
| chr16:566252-566652 | Rare:95 |