| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4476270-4476474 | Common:3; Rare:77 | ||||
| chr16:4538422-4538629 | Common:2; Rare:79 | ||||
| chr16:4693449-4693732 | Common:2; Rare:122 | ||||
| chr16:4734190-4734309 | Common:1; Rare:44 | ||||
| chr16:4847273-4847439 | Common:1; Rare:70 | ||||
| chr16:5033920-5033960 | Rare:16 | ||||
| chr16:8797612-8797925 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:10743718-10743872 | Rare:66 | ||||
| chr16:10877117-10877275 | Rare:31; Clinvar:3 | ||||
| chr16:11345195-11345454 | Common:1; Rare:76 | ||||
| chr16:11586896-11587083 | Common:3; Rare:52 | ||||
| chr16:11587171-11587417 | Common:1; Rare:65 | ||||
| chr16:11742723-11743000 | Common:1; Rare:114 | ||||
| chr16:11797184-11797499 | Common:2; Rare:120 | ||||
| chr16:11965014-11965219 | Common:2; Rare:48 |