| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66549813-66550001 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66550273-66550585 | Common:1; Rare:66; Clinvar:1 | ||||
| chr16:66552520-66552701 | Rare:72 | ||||
| chr16:66604609-66604681 | Rare:22 | ||||
| chr16:66751547-66751936 | Common:3; Rare:115 | ||||
| chr16:66880328-66880617 | Common:2; Rare:73 | ||||
| chr16:66925521-66925697 | Common:1; Rare:32 | ||||
| chr16:66934327-66934711 | Common:1; Rare:117 | ||||
| chr16:67000515-67000599 | Rare:21 | ||||
| chr16:67001046-67001337 | Common:4; Rare:77 | ||||
| chr16:67028978-67029118 | Rare:49 | ||||
| chr16:67109834-67110002 | Rare:53 | ||||
| chr16:67150954-67151022 | Rare:13 | ||||
| chr16:67159856-67160025 | Rare:29 | ||||
| chr16:67160983-67161134 | Rare:35 |