| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31459284-31459517 | Common:1; Rare:97 | ||||
| chr16:31508357-31508490 | Common:4; Rare:57 | ||||
| chr16:32253041-32253332 | Rare:25 | ||||
| chr16:46621316-46621502 | Rare:74 | ||||
| chr16:46689131-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689763 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973583-46973796 | Rare:98 | ||||
| chr16:47460972-47461383 | Common:2; Rare:170; Clinvar (benign):2 | ||||
| chr16:48244198-48244601 | Common:2; Rare:122 | ||||
| chr16:48365846-48366152 | Common:5; Rare:85 | ||||
| chr16:48385258-48385537 | Common:3; Rare:109 | ||||
| chr16:48609973-48610271 | Common:2; Rare:108 | ||||
| chr16:50025000-50025313 | Common:4; Rare:104 | ||||
| chr16:53054905-53055069 | Common:1; Rare:32 | ||||
| chr16:53099098-53099189 | Rare:20 |