| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27268713-27268912 | Common:2; Rare:121 | ||||
| chr16:27313794-27313985 | Common:4; Rare:111 | ||||
| chr16:27549861-27550212 | Common:4; Rare:261 | ||||
| chr16:28211808-28212154 | Common:6; Rare:249 | ||||
| chr16:28291970-28292600 | Common:4; Rare:232 | ||||
| chr16:28491190-28491650 | Common:3; Rare:171; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr16:28491873-28492694 | Common:11; Rare:343; Clinvar:10; Clinvar (benign):8 | ||||
| chr16:28538924-28539186 | Common:3; Rare:86 | ||||
| chr16:28553501-28554085 | Common:6; Rare:192 | ||||
| chr16:28554138-28554363 | Common:8; Rare:155 | ||||
| chr16:28623315-28623425 | Rare:40 | ||||
| chr16:28822568-28822786 | Rare:149 | ||||
| chr16:28822925-28823309 | Common:8; Rare:233 | ||||
| chr16:28823748-28824623 | Common:8; Rare:428 | ||||
| chr16:28845260-28845820 | Common:4; Rare:172; Clinvar (pathogenic):1 |