| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27549886-27550167 | Common:2; Rare:104 | ||||
| chr16:28491954-28492103 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28538789-28539189 | Common:2; Rare:94 | ||||
| chr16:28822543-28822752 | Common:1; Rare:77 | ||||
| chr16:28822925-28823125 | Common:3; Rare:58 | ||||
| chr16:28843751-28844072 | Rare:99; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:28846223-28846623 | Common:2; Rare:139; Clinvar:7; Clinvar (benign):6 | ||||
| chr16:28863724-28863979 | Common:3; Rare:65 | ||||
| chr16:28879887-28880023 | Common:2; Rare:43 | ||||
| chr16:28925167-28925412 | Rare:79 | ||||
| chr16:28974647-28974792 | Common:1; Rare:60 | ||||
| chr16:29454033-29454571 | |||||
| chr16:29678989-29679198 | Rare:66 | ||||
| chr16:29790515-29790794 | Common:1; Rare:114; Clinvar (benign):2 | ||||
| chr16:29805482-29805682 | Common:2; Rare:92 |