| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067808-19067920 | Common:2; Rare:27 | ||||
| chr16:20806317-20806490 | Rare:55 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21652600-21652846 | Rare:52 | ||||
| chr16:21953003-21953435 | Common:1; Rare:108; Clinvar (benign):3 | ||||
| chr16:22436990-22437145 | Rare:59 | ||||
| chr16:22437164-22437676 | Common:2; Rare:147 | ||||
| chr16:23557304-23557650 | Common:3; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641533 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729620-24729745 | Common:6; Rare:69 | ||||
| chr16:25111453-25111829 | Common:2; Rare:107 | ||||
| chr16:27268724-27268893 | Common:1; Rare:61 | ||||
| chr16:27549865-27550168 | Common:2; Rare:119 | ||||
| chr16:28494340-28494675 | Rare:65 | ||||
| chr16:28844020-28844245 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 |