| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443417-3443820 | Common:4; Rare:144 | ||||
| chr16:3611537-3611826 | Common:1; Rare:124; Clinvar:2 | ||||
| chr16:3717475-3717630 | Rare:76; Clinvar:1 | ||||
| chr16:4344134-4344402 | Common:2; Rare:43 | ||||
| chr16:4351232-4351685 | Common:5; Rare:159 | ||||
| chr16:4425725-4426035 | Common:1; Rare:149 | ||||
| chr16:4476270-4476490 | Common:3; Rare:80 | ||||
| chr16:4538419-4538582 | Common:1; Rare:56 | ||||
| chr16:4668156-4668438 | Common:2; Rare:104 | ||||
| chr16:4734128-4734542 | Common:1; Rare:138 | ||||
| chr16:4767126-4767322 | Common:1; Rare:64 | ||||
| chr16:4802281-4802771 | Common:1; Rare:219; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:4802827-4803204 | Common:4; Rare:174; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4843811-4843880 | Common:2; Rare:24 | ||||
| chr16:4847244-4847511 | Common:3; Rare:125 |