| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68023209-68023302 | Common:1; Rare:25 | ||||
| chr16:68245161-68245397 | Common:1; Rare:67 | ||||
| chr16:68264433-68264558 | Rare:40 | ||||
| chr16:68310911-68311116 | Common:1; Rare:103 | ||||
| chr16:68539170-68539323 | Common:1; Rare:76 | ||||
| chr16:69132510-69132689 | Rare:67 | ||||
| chr16:69339551-69339821 | Common:1; Rare:109; Clinvar (benign):1 | ||||
| chr16:69424485-69424689 | Common:1; Rare:59 | ||||
| chr16:69726437-69726733 | Common:3; Rare:79 | ||||
| chr16:69762152-69762381 | Common:1; Rare:65 | ||||
| chr16:70114124-70114376 | Common:3; Rare:91 | ||||
| chr16:70289446-70289646 | Rare:74; Clinvar:1 | ||||
| chr16:70346751-70346994 | Common:2; Rare:119 | ||||
| chr16:70454332-70454619 | Common:2; Rare:73 | ||||
| chr16:70523532-70523864 | Common:3; Rare:107; Clinvar (pathogenic):1 |