| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67528718-67528845 | Rare:33 | ||||
| chr16:67660222-67660398 | Rare:110; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660751-67661030 | Common:2; Rare:96 | ||||
| chr16:67719270-67719444 | Rare:45 | ||||
| chr16:67884728-67884909 | Rare:57 | ||||
| chr16:67935647-67935899 | Common:1; Rare:74 | ||||
| chr16:68023192-68023302 | Common:1; Rare:36 | ||||
| chr16:68245183-68245410 | Common:1; Rare:71 | ||||
| chr16:68264385-68264594 | Rare:68 | ||||
| chr16:68310742-68311150 | Common:5; Rare:181 | ||||
| chr16:68539156-68539327 | Common:2; Rare:85 | ||||
| chr16:68737123-68737418 | Common:4; Rare:97; Clinvar:5; Clinvar (benign):17 | ||||
| chr16:69132537-69132671 | Rare:55 | ||||
| chr16:69339541-69339831 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:69726448-69726548 | Rare:32 |