| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69385722-69385952 | Rare:77 | ||||
| chr16:69424345-69424698 | Common:2; Rare:95 | ||||
| chr16:69726382-69727137 | Common:4; Rare:202 | ||||
| chr16:69762251-69762566 | Common:3; Rare:101 | ||||
| chr16:70289408-70289629 | Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:70299132-70299267 | Rare:30 | ||||
| chr16:70346735-70346971 | Common:2; Rare:113 | ||||
| chr16:70454540-70454612 | Rare:16 | ||||
| chr16:70523517-70523861 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70523987-70524033 | Rare:10 | ||||
| chr16:71484104-71484380 | Common:2; Rare:73 | ||||
| chr16:71564930-71565016 | Rare:31 | ||||
| chr16:71565451-71565705 | Rare:45 | ||||
| chr16:71808772-71808879 | Common:1; Rare:59 | ||||
| chr16:71809042-71809339 | Common:3; Rare:95 |