| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28210926-28211294 | Common:3; Rare:127 | ||||
| chr16:28211814-28212367 | Common:10; Rare:423 | ||||
| chr16:28292025-28292171 | Rare:30 | ||||
| chr16:28292203-28292619 | Common:5; Rare:262 | ||||
| chr16:28491145-28491554 | Common:4; Rare:185; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:28491889-28492206 | Common:5; Rare:176; Clinvar:8; Clinvar (benign):6 | ||||
| chr16:28492217-28492343 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr16:28538712-28539296 | Common:5; Rare:231 | ||||
| chr16:28553668-28553990 | Common:3; Rare:83 | ||||
| chr16:28553913-28554056 | Common:3; Rare:48 | ||||
| chr16:28554064-28554395 | Common:12; Rare:288 | ||||
| chr16:28596999-28597399 | Common:3; Rare:174 | ||||
| chr16:28609960-28610454 | Common:10; Rare:171 | ||||
| chr16:28623160-28623490 | Rare:119 | ||||
| chr16:28822529-28823362 | Common:14; Rare:825 |