| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67846854-67847238 | Common:2; Rare:103 | ||||
| chr16:67968534-67968878 | Common:2; Rare:114 | ||||
| chr16:68023209-68023314 | Common:1; Rare:28 | ||||
| chr16:68245180-68245420 | Common:1; Rare:74 | ||||
| chr16:68264427-68264604 | Rare:59 | ||||
| chr16:68310915-68311081 | Common:1; Rare:83 | ||||
| chr16:69132113-69132344 | Rare:46 | ||||
| chr16:69132528-69132672 | Rare:56 | ||||
| chr16:69339548-69339841 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr16:69424340-69424695 | Common:3; Rare:93 | ||||
| chr16:69726435-69726796 | Common:4; Rare:97 | ||||
| chr16:69762288-69762387 | Rare:23 | ||||
| chr16:70114107-70114376 | Common:3; Rare:94 | ||||
| chr16:70346759-70346952 | Common:1; Rare:93 | ||||
| chr16:70523512-70523861 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |