| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4371715-4371848 | Rare:51 | ||||
| chr16:4425757-4425883 | Common:1; Rare:58 | ||||
| chr16:4476300-4476483 | Common:1; Rare:70 | ||||
| chr16:4538394-4538603 | Common:2; Rare:71 | ||||
| chr16:4538726-4538894 | Rare:64 | ||||
| chr16:4614877-4614989 | Rare:23 | ||||
| chr16:4624580-4624894 | Common:1; Rare:117 | ||||
| chr16:4693453-4693729 | Common:2; Rare:117 | ||||
| chr16:4734199-4734534 | Common:1; Rare:109 | ||||
| chr16:4767126-4767306 | Common:1; Rare:62 | ||||
| chr16:5033926-5033987 | Rare:22 | ||||
| chr16:5097740-5098032 | Common:4; Rare:98 | ||||
| chr16:8674396-8674661 | Common:1; Rare:98; Clinvar:2 | ||||
| chr16:8712880-8713157 | Common:4; Rare:73 | ||||
| chr16:8797618-8797866 | Rare:94; Clinvar:2; Clinvar (benign):1 |