| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065463-30065897 | Rare:142 | ||||
| chr16:30069511-30070029 | Common:1; Rare:194; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30096095-30096412 | Rare:87 | ||||
| chr16:30113538-30113642 | Rare:14 | ||||
| chr16:30123216-30123384 | Common:5; Rare:48 | ||||
| chr16:30534748-30535089 | Common:3; Rare:103 | ||||
| chr16:30697927-30698235 | Common:1; Rare:136 | ||||
| chr16:30698413-30698590 | Common:1; Rare:79 | ||||
| chr16:30762070-30762377 | Common:3; Rare:98 | ||||
| chr16:30787152-30787370 | Common:1; Rare:42 | ||||
| chr16:30893960-30894241 | Common:5; Rare:75 | ||||
| chr16:30923256-30923592 | Common:1; Rare:81 | ||||
| chr16:31033218-31033577 | Common:2; Rare:103 | ||||
| chr16:31074184-31074431 | Common:1; Rare:66 | ||||
| chr16:31459091-31459161 | Rare:23 |