| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47460884-47461383 | Common:2; Rare:204; Clinvar (benign):2 | ||||
| chr16:48244254-48244566 | Common:2; Rare:94 | ||||
| chr16:48385258-48385575 | Common:3; Rare:123 | ||||
| chr16:48609968-48610382 | Common:3; Rare:134 | ||||
| chr16:49281823-49282068 | Rare:70 | ||||
| chr16:50024943-50025318 | Common:5; Rare:117 | ||||
| chr16:50065816-50065996 | Common:5; Rare:63 | ||||
| chr16:50066222-50066453 | Common:3; Rare:121 | ||||
| chr16:50741674-50742207 | Common:7; Rare:168; Clinvar:1 | ||||
| chr16:53208305-53208694 | Rare:67 | ||||
| chr16:53703809-53704238 | Common:1; Rare:139; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:56191063-56191864 | Common:7; Rare:249 | ||||
| chr16:56191986-56192353 | Common:1; Rare:66; Clinvar (benign):3 | ||||
| chr16:56451287-56451651 | Common:2; Rare:122 | ||||
| chr16:56519966-56520174 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):5 |