| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70523496-70523882 | Common:3; Rare:135; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71289174-71289232 | Rare:14 | ||||
| chr16:71289292-71289468 | Common:2; Rare:55 | ||||
| chr16:71564930-71565021 | Rare:31 | ||||
| chr16:71808751-71808869 | Common:1; Rare:61 | ||||
| chr16:71809048-71809323 | Common:3; Rare:92 | ||||
| chr16:71845879-71846022 | Common:2; Rare:49 | ||||
| chr16:71895301-71895578 | Common:3; Rare:99 | ||||
| chr16:72008505-72008772 | Common:5; Rare:99; Clinvar (benign):1 | ||||
| chr16:72093579-72094002 | Common:1; Rare:105 | ||||
| chr16:74296655-74296920 | Rare:109 | ||||
| chr16:74607080-74607211 | Rare:67 | ||||
| chr16:74666847-74667186 | Common:4; Rare:108 | ||||
| chr16:74701140-74701343 | Common:1; Rare:47 | ||||
| chr16:74985094-74985358 | Common:2; Rare:81 |