| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71808778-71808885 | Common:1; Rare:59 | ||||
| chr16:71809010-71809345 | Common:3; Rare:105 | ||||
| chr16:71845890-71846023 | Common:2; Rare:43 | ||||
| chr16:71895227-71895584 | Common:3; Rare:144 | ||||
| chr16:72093573-72093934 | Rare:90 | ||||
| chr16:74296700-74296987 | Rare:111 | ||||
| chr16:74304024-74304393 | Common:2; Rare:83 | ||||
| chr16:74606810-74607197 | Rare:193 | ||||
| chr16:74700845-74701248 | Common:4; Rare:75 | ||||
| chr16:75116726-75116854 | Common:2; Rare:32 | ||||
| chr16:75433339-75433798 | Common:4; Rare:151 | ||||
| chr16:75464379-75464454 | Common:2; Rare:30 | ||||
| chr16:75623222-75623370 | Common:3; Rare:53 | ||||
| chr16:75647614-75647848 | Common:3; Rare:118; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648015-75648442 | Rare:162 |