| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88732494-88732805 | Common:2; Rare:158; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:88811883-88812032 | Common:2; Rare:72; Clinvar (benign):1 | ||||
| chr16:88856882-88857162 | Common:4; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88976953-88977249 | Common:1; Rare:82 | ||||
| chr16:89217619-89217750 | Common:1; Rare:62 | ||||
| chr16:89508296-89508428 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560555-89560717 | Rare:68 | ||||
| chr16:89657637-89658140 | Common:4; Rare:250 | ||||
| chr16:89686520-89686704 | Common:7; Rare:75 | ||||
| chr16:89686895-89687094 | Common:3; Rare:77 | ||||
| chr16:89719377-89719643 | Common:4; Rare:80 | ||||
| chr16:89720678-89721030 | Common:1; Rare:117 | ||||
| chr16:89816611-89816769 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:89873440-89873789 | Common:5; Rare:163 | ||||
| chr16:89873802-89873878 | Common:1; Rare:25 |