| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58392738-58392945 | Common:4; Rare:87 | ||||
| chr16:58515251-58515539 | Common:8; Rare:145 | ||||
| chr16:58629737-58630165 | Common:4; Rare:177 | ||||
| chr16:58684698-58684820 | Rare:36 | ||||
| chr16:58734236-58734394 | Common:7; Rare:97 | ||||
| chr16:66378863-66379054 | Common:2; Rare:40 | ||||
| chr16:66549700-66550050 | Common:6; Rare:181; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:66550059-66550404 | Common:4; Rare:205; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:66552445-66552832 | Rare:252 | ||||
| chr16:66696634-66696982 | Common:10; Rare:251 | ||||
| chr16:66750810-66751420 | Common:3; Rare:238 | ||||
| chr16:66751568-66752060 | Common:4; Rare:164 | ||||
| chr16:66830901-66831067 | Rare:73 | ||||
| chr16:66880324-66880658 | Common:4; Rare:156 | ||||
| chr16:66933960-66934280 | Common:2; Rare:194 |