| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30893953-30894289 | Common:5; Rare:88 | ||||
| chr16:30922582-30922847 | Common:1; Rare:75 | ||||
| chr16:30923242-30923598 | Common:1; Rare:87 | ||||
| chr16:31033453-31033628 | Common:1; Rare:64 | ||||
| chr16:31074184-31074453 | Common:1; Rare:75 | ||||
| chr16:31190121-31190399 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31471943-31472200 | Rare:60 | ||||
| chr16:46689132-46689312 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689516-46689714 | Common:2; Rare:82; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973632-46973771 | Rare:66 | ||||
| chr16:47460903-47461403 | Common:3; Rare:202; Clinvar (benign):3 | ||||
| chr16:48610178-48610319 | Common:2; Rare:61 | ||||
| chr16:53054840-53055055 | Common:1; Rare:50 | ||||
| chr16:53703809-53704219 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:55479049-55479422 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):1 |