| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88704076-88704292 | Common:3; Rare:58 | ||||
| chr16:88706310-88706606 | Common:5; Rare:145 | ||||
| chr16:88785152-88785355 | Common:1; Rare:79 | ||||
| chr16:88785494-88785723 | Rare:59 | ||||
| chr16:88802642-88803161 | Common:13; Rare:128 | ||||
| chr16:88803529-88803866 | Common:6; Rare:148 | ||||
| chr16:88804585-88804639 | Rare:30; Clinvar (benign):1 | ||||
| chr16:88811346-88811606 | Common:2; Rare:92; Clinvar:1 | ||||
| chr16:88811802-88812105 | Common:2; Rare:125; Clinvar (benign):1 | ||||
| chr16:88812135-88812546 | Common:6; Rare:135 | ||||
| chr16:88856468-88856810 | Common:5; Rare:99; Clinvar (pathogenic):2 | ||||
| chr16:88856860-88857209 | Common:4; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88976898-88977319 | Common:1; Rare:116 | ||||
| chr16:88977503-88977679 | Common:1; Rare:43 | ||||
| chr16:89093698-89093979 | Common:6; Rare:115 |