| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70523517-70523886 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70523953-70523993 | Rare:4 | ||||
| chr16:71289205-71289693 | Common:5; Rare:150 | ||||
| chr16:71808751-71808878 | Common:1; Rare:67 | ||||
| chr16:71809034-71809348 | Common:3; Rare:99 | ||||
| chr16:71845904-71846017 | Common:2; Rare:35 | ||||
| chr16:71895306-71895588 | Common:3; Rare:103 | ||||
| chr16:72008505-72008844 | Common:6; Rare:137; Clinvar (benign):2 | ||||
| chr16:72093449-72093957 | Rare:127 | ||||
| chr16:74296460-74296984 | Common:1; Rare:174 | ||||
| chr16:74607090-74607232 | Rare:73 | ||||
| chr16:74666822-74667217 | Common:7; Rare:122 | ||||
| chr16:74985021-74985291 | Common:2; Rare:93 | ||||
| chr16:75148391-75148603 | Common:4; Rare:95 | ||||
| chr16:75265874-75266037 | Common:3; Rare:77 |