| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69762266-69762381 | Common:1; Rare:28 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70346759-70346952 | Common:1; Rare:93 | ||||
| chr16:70454543-70454638 | Rare:25 | ||||
| chr16:70523530-70523837 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr16:71289174-71289465 | Common:2; Rare:78 | ||||
| chr16:71564926-71565015 | Rare:31 | ||||
| chr16:71808774-71809268 | Common:4; Rare:189 | ||||
| chr16:71845920-71846029 | Common:1; Rare:35 | ||||
| chr16:71895254-71895584 | Common:3; Rare:126 | ||||
| chr16:72054432-72054634 | Common:4; Rare:67 | ||||
| chr16:72093579-72093934 | Rare:89 | ||||
| chr16:74296460-74296984 | Common:1; Rare:174 | ||||
| chr16:74304197-74304375 | Common:2; Rare:41 | ||||
| chr16:74607017-74607206 | Rare:100 |