| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29995606-29995704 | Rare:43 | ||||
| chr16:29996073-29996296 | Common:2; Rare:78 | ||||
| chr16:30065475-30065845 | Rare:126 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30534824-30535084 | Common:2; Rare:82 | ||||
| chr16:30762056-30762333 | Common:3; Rare:93 | ||||
| chr16:30893972-30894294 | Common:5; Rare:84 | ||||
| chr16:31074213-31074450 | Common:1; Rare:64 | ||||
| chr16:31472113-31472191 | Rare:21 | ||||
| chr16:31508389-31508450 | Rare:23 | ||||
| chr16:46689134-46689386 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973568-46973750 | Rare:78 | ||||
| chr16:47461041-47461343 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr16:53054828-53055048 | Common:2; Rare:54 | ||||
| chr16:53703821-53704179 | Rare:101; Clinvar:3; Clinvar (benign):1 |