| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3575759-3576658 | Common:7; Rare:282 | ||||
| chr16:3578211-3578403 | Rare:44 | ||||
| chr16:3578870-3579340 | Common:9; Rare:232 | ||||
| chr16:3587460-3587800 | Common:4; Rare:76 | ||||
| chr16:3610275-3610693 | Rare:170 | ||||
| chr16:3623781-3624065 | Rare:67 | ||||
| chr16:3626049-3626540 | Common:4; Rare:177 | ||||
| chr16:3637423-3637752 | Rare:73 | ||||
| chr16:3798000-3798490 | Common:1; Rare:103 | ||||
| chr16:3807686-3808151 | Rare:138 | ||||
| chr16:3810180-3810947 | Common:4; Rare:335; Clinvar:2; Clinvar (benign):8 | ||||
| chr16:3856459-3856859 | Common:2; Rare:105 | ||||
| chr16:4183040-4183400 | Common:9; Rare:123 | ||||
| chr16:4183338-4183461 | Rare:30 | ||||
| chr16:4183928-4184097 | Common:2; Rare:126 |