| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28823993-28824094 | Rare:24 | ||||
| chr16:28824116-28824426 | Common:4; Rare:96 | ||||
| chr16:28846308-28846619 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:28863320-28863585 | Common:1; Rare:57 | ||||
| chr16:28925172-28925261 | Rare:22 | ||||
| chr16:29745878-29746255 | Common:2; Rare:71 | ||||
| chr16:29805325-29805782 | Common:2; Rare:211 | ||||
| chr16:29807804-29808153 | Common:2; Rare:191 | ||||
| chr16:29962775-29962916 | Common:1; Rare:27 | ||||
| chr16:29995606-29995714 | Rare:49 | ||||
| chr16:29996032-29996283 | Common:2; Rare:85 | ||||
| chr16:30065747-30065861 | Rare:46 | ||||
| chr16:30069535-30070029 | Common:1; Rare:181; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075939-30076398 | Common:3; Rare:139 | ||||
| chr16:30187026-30187449 | Rare:142; Clinvar:1; Clinvar (benign):1 |