| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:32253701-32253851 | Rare:73 | ||||
| chr16:32253890-32254231 | Common:3; Rare:47 | ||||
| chr16:46621325-46621480 | Rare:55 | ||||
| chr16:46678951-46679432 | Rare:81; Clinvar:1 | ||||
| chr16:46689108-46689416 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689834 | Common:2; Rare:136; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46789926-46790035 | Common:4; Rare:19 | ||||
| chr16:46831111-46831409 | Common:2; Rare:105 | ||||
| chr16:46973201-46973403 | Rare:54 | ||||
| chr16:46973524-46973796 | Rare:110 | ||||
| chr16:47460837-47460911 | Rare:24 | ||||
| chr16:47460924-47461378 | Common:2; Rare:185; Clinvar (benign):2 | ||||
| chr16:48091212-48091244 | Rare:17 | ||||
| chr16:48223658-48223728 | Rare:15 | ||||
| chr16:48244254-48244571 | Common:2; Rare:95 |