| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68539110-68539379 | Common:2; Rare:121 | ||||
| chr16:69132547-69132686 | Rare:58 | ||||
| chr16:69311105-69311411 | Rare:92 | ||||
| chr16:69339503-69339807 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69424340-69424686 | Common:2; Rare:90 | ||||
| chr16:69726435-69726523 | Common:1; Rare:29 | ||||
| chr16:69762284-69762381 | Rare:23 | ||||
| chr16:70114136-70114376 | Common:3; Rare:84 | ||||
| chr16:70299125-70299244 | Rare:25 | ||||
| chr16:70346834-70346945 | Common:1; Rare:53 | ||||
| chr16:70523538-70523844 | Common:3; Rare:96 | ||||
| chr16:71289342-71289673 | Common:2; Rare:110 | ||||
| chr16:71845905-71846023 | Common:1; Rare:37 | ||||
| chr16:71895313-71895574 | Common:2; Rare:97 | ||||
| chr16:72008576-72008772 | Common:2; Rare:66; Clinvar (benign):1 |