| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50066234-50066447 | Common:3; Rare:115 | ||||
| chr16:50152642-50152943 | Common:5; Rare:86 | ||||
| chr16:50266452-50266587 | Common:1; Rare:39 | ||||
| chr16:50313342-50313573 | Common:10; Rare:60 | ||||
| chr16:50681218-50681406 | Common:1; Rare:40 | ||||
| chr16:50693474-50693631 | Common:1; Rare:66 | ||||
| chr16:50741708-50742210 | Common:7; Rare:158; Clinvar:1 | ||||
| chr16:50742715-50742782 | Rare:15 | ||||
| chr16:53054916-53055048 | Common:1; Rare:26 | ||||
| chr16:53099002-53099228 | Rare:43 | ||||
| chr16:53434677-53434735 | Common:1; Rare:19 | ||||
| chr16:53435473-53435646 | Common:1; Rare:34 | ||||
| chr16:53703821-53703975 | Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:53703990-53704227 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:56451102-56451123 | Rare:6 |