| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3065197-3065494 | Common:5; Rare:80 | ||||
| chr16:3112556-3112665 | Common:2; Rare:26 | ||||
| chr16:3134841-3135143 | Common:3; Rare:79 | ||||
| chr16:3263665-3263823 | Common:1; Rare:40 | ||||
| chr16:3305397-3305514 | Common:1; Rare:40 | ||||
| chr16:3400955-3401244 | Common:6; Rare:108 | ||||
| chr16:3443441-3443729 | Common:3; Rare:99 | ||||
| chr16:3457908-3458120 | Common:2; Rare:103 | ||||
| chr16:3611594-3611784 | Rare:81 | ||||
| chr16:4425763-4425907 | Common:1; Rare:77 | ||||
| chr16:4476271-4476480 | Common:3; Rare:79 | ||||
| chr16:4734224-4734538 | Rare:97 | ||||
| chr16:4767146-4767253 | Rare:37 | ||||
| chr16:5071782-5071852 | Rare:33; Clinvar (benign):1 | ||||
| chr16:8797610-8797885 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |