| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70523527-70523872 | Common:3; Rare:115; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71289205-71289468 | Common:2; Rare:72 | ||||
| chr16:71564926-71565029 | Rare:34 | ||||
| chr16:71723815-71724098 | Common:5; Rare:99 | ||||
| chr16:71808331-71808469 | Rare:45 | ||||
| chr16:71808754-71808885 | Common:1; Rare:68 | ||||
| chr16:71808970-71809308 | Common:3; Rare:115 | ||||
| chr16:71845905-71846029 | Common:1; Rare:39 | ||||
| chr16:71895219-71895584 | Common:3; Rare:146 | ||||
| chr16:72008517-72008765 | Common:5; Rare:90; Clinvar (benign):1 | ||||
| chr16:72013939-72014054 | Common:1; Rare:25 | ||||
| chr16:72014122-72014590 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr16:72056062-72056243 | Rare:85 | ||||
| chr16:72093443-72094046 | Common:1; Rare:146 | ||||
| chr16:74296722-74296941 | Rare:93 |