| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355233-30355438 | Common:1; Rare:72 | ||||
| chr16:30534838-30535078 | Common:2; Rare:79 | ||||
| chr16:30893945-30894242 | Common:5; Rare:82 | ||||
| chr16:31033453-31033741 | Common:1; Rare:87 | ||||
| chr16:31074299-31074454 | Rare:43 | ||||
| chr16:31508371-31508454 | Rare:33 | ||||
| chr16:46689111-46689327 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689709 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973644-46973771 | Rare:58 | ||||
| chr16:47461051-47461343 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr16:50245930-50246174 | Common:2; Rare:56 | ||||
| chr16:53703830-53704221 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286722-54286968 | Common:1; Rare:70 | ||||
| chr16:56451140-56451633 | Common:3; Rare:163 | ||||
| chr16:56729949-56730186 | Common:1; Rare:56 |