| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726453-69726534 | Rare:27 | ||||
| chr16:69726548-69726785 | Common:3; Rare:53 | ||||
| chr16:70114115-70114393 | Common:3; Rare:99 | ||||
| chr16:70299147-70299239 | Rare:22 | ||||
| chr16:70346804-70346982 | Common:2; Rare:91 | ||||
| chr16:70454513-70454619 | Common:1; Rare:32 | ||||
| chr16:70523533-70523837 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr16:70680010-70680344 | Common:2; Rare:103 | ||||
| chr16:71564930-71565015 | Rare:31 | ||||
| chr16:71808778-71809129 | Common:1; Rare:150 | ||||
| chr16:71845890-71846023 | Common:2; Rare:43 | ||||
| chr16:71895250-71895574 | Common:2; Rare:126 | ||||
| chr16:72008576-72008760 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr16:72054615-72054627 | Rare:3 | ||||
| chr16:72093443-72093986 | Common:1; Rare:136 |