| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70479339-70479609 | Common:2; Rare:81 | ||||
| chr16:71670502-71670847 | Common:3; Rare:75 | ||||
| chr16:71723226-71723258 | Rare:11 | ||||
| chr16:72098769-72099045 | Common:1; Rare:89 | ||||
| chr16:72099566-72099885 | Common:1; Rare:105; Clinvar (pathogenic):1 | ||||
| chr16:72107506-72107718 | Rare:75 | ||||
| chr16:72664938-72665192 | Common:1; Rare:83 | ||||
| chr16:74302161-74302277 | Rare:35 | ||||
| chr16:74305021-74305538 | Rare:140 | ||||
| chr16:74331122-74331159 | Rare:8 | ||||
| chr16:74368124-74368376 | Common:1; Rare:70 | ||||
| chr16:75239702-75239823 | Common:2; Rare:27 | ||||
| chr16:75241968-75242022 | Common:1; Rare:15 | ||||
| chr16:75502119-75502343 | Common:2; Rare:36 | ||||
| chr16:75525945-75526082 | Rare:27 |