| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68310922-68311084 | Common:1; Rare:80 | ||||
| chr16:69132514-69132672 | Rare:58 | ||||
| chr16:69339551-69339847 | Common:1; Rare:128; Clinvar (benign):1 | ||||
| chr16:69424478-69424681 | Rare:59 | ||||
| chr16:69726437-69726802 | Common:3; Rare:97 | ||||
| chr16:70289476-70289656 | Rare:64; Clinvar:1 | ||||
| chr16:70523524-70523847 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71895444-71895540 | Rare:21 | ||||
| chr16:72008528-72008766 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr16:72093602-72093934 | Rare:77 | ||||
| chr16:74666875-74667057 | Common:1; Rare:67 | ||||
| chr16:75433452-75433798 | Common:4; Rare:99 | ||||
| chr16:75647613-75647884 | Common:4; Rare:140; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190680-77190998 | Common:12; Rare:102 | ||||
| chr16:77191128-77191211 | Common:1; Rare:37 |