| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3282783-3283020 | Common:2; Rare:77 | ||||
| chr16:3283030-3283639 | Common:8; Rare:162 | ||||
| chr16:3305095-3305649 | Common:7; Rare:179 | ||||
| chr16:3305698-3305832 | Rare:44 | ||||
| chr16:3364817-3365293 | Common:9; Rare:145 | ||||
| chr16:3400884-3401349 | Common:8; Rare:165 | ||||
| chr16:3443396-3443756 | Common:3; Rare:126 | ||||
| chr16:3444100-3444156 | Rare:10 | ||||
| chr16:3444163-3444349 | Common:3; Rare:45 | ||||
| chr16:3457537-3457728 | Common:1; Rare:46 | ||||
| chr16:3457810-3458194 | Common:3; Rare:158 | ||||
| chr16:3500785-3501083 | Common:5; Rare:110 | ||||
| chr16:3611442-3611885 | Common:2; Rare:174; Clinvar:2 | ||||
| chr16:3716728-3717071 | Common:1; Rare:99 | ||||
| chr16:3717273-3717886 | Common:1; Rare:229; Clinvar:1; Clinvar (benign):1 |