| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442769-31443059 | Common:1; Rare:47 | ||||
| chr16:31459310-31459517 | Common:1; Rare:85 | ||||
| chr16:31471882-31472191 | Rare:68 | ||||
| chr16:31508374-31508516 | Common:4; Rare:58 | ||||
| chr16:46689130-46689313 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689512-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973606-46973753 | Rare:68 | ||||
| chr16:47461035-47461378 | Common:2; Rare:132; Clinvar (benign):2 | ||||
| chr16:48244254-48244379 | Common:1; Rare:45 | ||||
| chr16:53208347-53208498 | Rare:31 | ||||
| chr16:53435506-53435634 | Common:1; Rare:23 | ||||
| chr16:53703809-53704208 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56451296-56451618 | Common:1; Rare:107 | ||||
| chr16:56519966-56520167 | Common:4; Rare:69; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608379-56608803 | Common:3; Rare:125 |