| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68310849-68311084 | Common:2; Rare:126 | ||||
| chr16:68530008-68530146 | Common:4; Rare:67 | ||||
| chr16:68539169-68539379 | Common:1; Rare:95 | ||||
| chr16:68808514-68808848 | Common:2; Rare:77; Clinvar:21; Clinvar (benign):18; Clinvar (pathogenic):1 | ||||
| chr16:68823131-68823605 | Common:4; Rare:105; Clinvar:25; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
| chr16:69106071-69106243 | Common:1; Rare:51 | ||||
| chr16:69132532-69132689 | Rare:63 | ||||
| chr16:69187041-69187199 | Rare:62 | ||||
| chr16:69339548-69339834 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr16:69424449-69424732 | Common:2; Rare:85 | ||||
| chr16:69565702-69566015 | Common:4; Rare:128 | ||||
| chr16:69566213-69566329 | Common:1; Rare:32 | ||||
| chr16:69726403-69726800 | Common:4; Rare:113 | ||||
| chr16:69754875-69755116 | Rare:88 | ||||
| chr16:69762279-69762387 | Common:1; Rare:26 |