| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88802989-88803161 | Common:4; Rare:47 | ||||
| chr16:88803557-88803840 | Common:5; Rare:131 | ||||
| chr16:88804585-88804644 | Rare:32; Clinvar (benign):1 | ||||
| chr16:88811330-88811588 | Common:2; Rare:91; Clinvar:1 | ||||
| chr16:88811861-88812222 | Common:2; Rare:138; Clinvar (benign):1 | ||||
| chr16:88856875-88857206 | Common:4; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88977073-88977325 | Rare:67 | ||||
| chr16:88977500-88977679 | Common:1; Rare:43 | ||||
| chr16:89093714-89093959 | Common:5; Rare:105 | ||||
| chr16:89217378-89217807 | Common:4; Rare:177 | ||||
| chr16:89320038-89320174 | Common:1; Rare:19 | ||||
| chr16:89489182-89489385 | Common:6; Rare:93 | ||||
| chr16:89490504-89491004 | Common:6; Rare:183 | ||||
| chr16:89491670-89491769 | Rare:22 | ||||
| chr16:89508214-89508474 | Common:2; Rare:139; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |