| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88453091-88453347 | Common:1; Rare:97 | ||||
| chr16:88570162-88570473 | Common:2; Rare:118 | ||||
| chr16:88663011-88663420 | Common:11; Rare:182 | ||||
| chr16:88686487-88686794 | Common:3; Rare:94 | ||||
| chr16:88706357-88706547 | Common:3; Rare:93 | ||||
| chr16:88803583-88803822 | Common:5; Rare:106 | ||||
| chr16:88811884-88812156 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr16:88856776-88857178 | Common:4; Rare:189; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88940420-88941331 | Common:2; Rare:431 | ||||
| chr16:89093470-89093990 | Common:14; Rare:180 | ||||
| chr16:89217591-89217733 | Common:1; Rare:68 | ||||
| chr16:89279947-89280527 | Common:5; Rare:480; Clinvar:15; Clinvar (benign):23; Clinvar (pathogenic):3 | ||||
| chr16:89490534-89490986 | Common:6; Rare:158 | ||||
| chr16:89491457-89492050 | Common:3; Rare:172 | ||||
| chr16:89508251-89508455 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |