| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68245161-68245397 | Common:1; Rare:67 | ||||
| chr16:68310922-68311081 | Common:1; Rare:79 | ||||
| chr16:68539151-68539342 | Common:2; Rare:91 | ||||
| chr16:69132532-69132671 | Rare:56 | ||||
| chr16:69187000-69187156 | Rare:54 | ||||
| chr16:69339548-69339826 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr16:69424489-69424797 | Common:1; Rare:97 | ||||
| chr16:69565849-69565989 | Common:2; Rare:57 | ||||
| chr16:69726446-69726785 | Common:3; Rare:87 | ||||
| chr16:69762282-69762367 | Rare:19 | ||||
| chr16:70114089-70114378 | Common:3; Rare:98 | ||||
| chr16:70289446-70289656 | Rare:77; Clinvar:1 | ||||
| chr16:70346809-70346978 | Common:2; Rare:85 | ||||
| chr16:70454484-70454619 | Common:1; Rare:42 | ||||
| chr16:70523533-70523872 | Common:3; Rare:112; Clinvar (pathogenic):1 |