| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30893963-30894275 | Common:5; Rare:81 | ||||
| chr16:30923242-30923556 | Common:1; Rare:81 | ||||
| chr16:31033235-31033608 | Common:2; Rare:110 | ||||
| chr16:31073726-31073847 | Rare:37 | ||||
| chr16:31074184-31074456 | Common:1; Rare:75 | ||||
| chr16:31108284-31108477 | Rare:44 | ||||
| chr16:31213920-31214172 | Common:1; Rare:40 | ||||
| chr16:31442805-31443059 | Common:1; Rare:39 | ||||
| chr16:31471931-31472186 | Rare:58 | ||||
| chr16:31508365-31508516 | Common:4; Rare:64 | ||||
| chr16:46621316-46621533 | Rare:78 | ||||
| chr16:46689134-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689457-46689714 | Common:2; Rare:95; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973581-46973775 | Rare:87 | ||||
| chr16:47461035-47461343 | Common:2; Rare:107; Clinvar (benign):1 |