| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:642850-643065 | Common:1; Rare:51 | ||||
| chr16:649233-649404 | Common:2; Rare:64 | ||||
| chr16:680324-680493 | Common:2; Rare:58 | ||||
| chr16:681149-681542 | Rare:124; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr16:684328-684499 | Common:3; Rare:96 | ||||
| chr16:690346-690439 | Common:1; Rare:43 | ||||
| chr16:695297-695426 | Common:3; Rare:59 | ||||
| chr16:721053-721179 | Common:2; Rare:30 | ||||
| chr16:737368-737592 | Common:1; Rare:54 | ||||
| chr16:740910-741108 | Common:1; Rare:70 | ||||
| chr16:760967-761134 | Common:2; Rare:55 | ||||
| chr16:970856-971192 | Common:7; Rare:153 | ||||
| chr16:1225241-1225413 | Common:3; Rare:87 | ||||
| chr16:1225747-1225841 | Common:2; Rare:38 | ||||
| chr16:1309381-1309727 | Rare:128 |