| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67806517-67806851 | Rare:71 | ||||
| chr16:67935707-67935871 | Rare:42 | ||||
| chr16:68023209-68023302 | Common:1; Rare:25 | ||||
| chr16:68245163-68245424 | Common:1; Rare:78 | ||||
| chr16:68264418-68264564 | Rare:50 | ||||
| chr16:68310915-68311062 | Common:1; Rare:71 | ||||
| chr16:69132547-69132678 | Rare:56 | ||||
| chr16:69339559-69339823 | Common:1; Rare:107; Clinvar (benign):1 | ||||
| chr16:69726437-69726812 | Common:3; Rare:98 | ||||
| chr16:70289440-70289761 | Common:2; Rare:131; Clinvar:1 | ||||
| chr16:70523533-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71808778-71809123 | Common:1; Rare:146 | ||||
| chr16:72093602-72093934 | Rare:77 | ||||
| chr16:74296730-74296895 | Rare:68 | ||||
| chr16:74607060-74607312 | Rare:129 |