| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67936791-67936923 | Common:1; Rare:23 | ||||
| chr16:67942748-67942892 | Common:1; Rare:39; Clinvar (pathogenic):1 | ||||
| chr16:67968576-67968864 | Common:2; Rare:95 | ||||
| chr16:68023207-68023329 | Common:1; Rare:32 | ||||
| chr16:68085137-68085486 | Common:3; Rare:78 | ||||
| chr16:68234383-68234804 | Rare:66 | ||||
| chr16:68245161-68245420 | Common:1; Rare:77 | ||||
| chr16:68264419-68264573 | Rare:54 | ||||
| chr16:68310874-68311089 | Common:1; Rare:113 | ||||
| chr16:68529981-68530138 | Common:5; Rare:79 | ||||
| chr16:68539168-68539330 | Common:1; Rare:82 | ||||
| chr16:68770761-68770995 | Rare:45 | ||||
| chr16:69132512-69132680 | Rare:63 | ||||
| chr16:69339499-69339823 | Common:2; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69424334-69424737 | Common:3; Rare:111 |