| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29805376-29805757 | Common:2; Rare:175 | ||||
| chr16:29862997-29863551 | Common:1; Rare:148 | ||||
| chr16:29962815-29962898 | Common:1; Rare:19 | ||||
| chr16:29995590-29995719 | Common:1; Rare:59 | ||||
| chr16:29996066-29996296 | Common:2; Rare:81 | ||||
| chr16:30355219-30355437 | Common:1; Rare:78 | ||||
| chr16:30534833-30535094 | Common:3; Rare:85 | ||||
| chr16:30698469-30698640 | Common:1; Rare:67 | ||||
| chr16:30893966-30894277 | Common:5; Rare:81 | ||||
| chr16:31074182-31074456 | Common:2; Rare:75 | ||||
| chr16:31183927-31184285 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:31459308-31459522 | Common:1; Rare:89 | ||||
| chr16:31471954-31472194 | Rare:58 | ||||
| chr16:31508371-31508477 | Common:1; Rare:41 | ||||
| chr16:46689126-46689396 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):1 |