| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31033440-31033588 | Common:1; Rare:58 | ||||
| chr16:31073701-31073848 | Rare:47 | ||||
| chr16:31074172-31074450 | Common:2; Rare:79 | ||||
| chr16:31094699-31094997 | Rare:87; Clinvar:1 | ||||
| chr16:31442757-31443063 | Common:1; Rare:50 | ||||
| chr16:31459091-31459188 | Rare:31 | ||||
| chr16:31459353-31459517 | Common:1; Rare:66 | ||||
| chr16:31471901-31472201 | Rare:70 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689130-46689381 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46789926-46790084 | Common:4; Rare:39 | ||||
| chr16:46973598-46973781 | Rare:81 | ||||
| chr16:47460976-47461374 | Common:2; Rare:164; Clinvar (benign):2 | ||||
| chr16:48244253-48244590 | Common:2; Rare:101 | ||||
| chr16:48385283-48385523 | Common:3; Rare:95 |