| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31873628-31873926 | Common:1; Rare:96 | ||||
| chr16:46689111-46689329 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:46689495-46689724 | Common:4; Rare:185; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:46789830-46790230 | Common:9; Rare:132 | ||||
| chr16:46831353-46831599 | Common:2; Rare:128 | ||||
| chr16:46883886-46884529 | Common:10; Rare:292 | ||||
| chr16:46915344-46915790 | Common:7; Rare:148 | ||||
| chr16:46972657-46973239 | Common:2; Rare:202 | ||||
| chr16:46973554-46973801 | Rare:199 | ||||
| chr16:47143935-47144102 | Rare:153 | ||||
| chr16:47460960-47461399 | Common:5; Rare:322; Clinvar (benign):5 | ||||
| chr16:47499560-47499860 | Rare:132; Clinvar:6; Clinvar (benign):2 | ||||
| chr16:48235460-48236058 | Common:4; Rare:153 | ||||
| chr16:48244184-48244572 | Common:5; Rare:185 | ||||
| chr16:48365850-48366144 | Common:10; Rare:147 |