| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10580569-10580864 | Common:2; Rare:99 | ||||
| chr16:11851515-11851645 | Rare:62 | ||||
| chr16:11976648-11976766 | Rare:43 | ||||
| chr16:15094247-15094389 | Rare:71 | ||||
| chr16:15650061-15650293 | Common:1; Rare:118 | ||||
| chr16:18801533-18801830 | Common:4; Rare:89 | ||||
| chr16:19067455-19067696 | Common:5; Rare:101; Clinvar:1 | ||||
| chr16:19067808-19067920 | Common:2; Rare:27 | ||||
| chr16:20806337-20806530 | Rare:69 | ||||
| chr16:20900515-20900819 | Common:1; Rare:71 | ||||
| chr16:21953038-21953413 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr16:23557343-23557557 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:25015339-25015461 | Common:2; Rare:43 | ||||
| chr16:25111478-25111796 | Common:2; Rare:82 |