| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69330580-69330778 | Common:2; Rare:80 | ||||
| chr16:69339532-69339841 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69726453-69726856 | Common:3; Rare:103 | ||||
| chr16:70289434-70289624 | Rare:71; Clinvar:1 | ||||
| chr16:70346759-70346951 | Common:1; Rare:93 | ||||
| chr16:70454513-70454619 | Common:1; Rare:32 | ||||
| chr16:70523524-70523861 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71808840-71809251 | Common:4; Rare:146 | ||||
| chr16:71845879-71846023 | Common:2; Rare:49 | ||||
| chr16:71895254-71895559 | Common:2; Rare:113 | ||||
| chr16:72093598-72093950 | Rare:84 | ||||
| chr16:73059080-73059132 | Rare:8 | ||||
| chr16:74296749-74296983 | Rare:94 | ||||
| chr16:74666863-74667090 | Common:1; Rare:75 | ||||
| chr16:75433291-75433797 | Common:4; Rare:173 |