| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27549432-27549832 | Common:1; Rare:115 | ||||
| chr16:27549832-27550243 | Common:14; Rare:910 | ||||
| chr16:27887346-27887746 | Common:5; Rare:100 | ||||
| chr16:28210992-28211392 | Common:6; Rare:155 | ||||
| chr16:28211507-28212382 | Common:27; Rare:956 | ||||
| chr16:28291900-28292150 | Common:2; Rare:88 | ||||
| chr16:28292170-28292600 | Common:2; Rare:102 | ||||
| chr16:28491121-28491521 | Common:4; Rare:158; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:28491518-28492551 | Common:19; Rare:637; Clinvar:24; Clinvar (benign):23; Clinvar (pathogenic):3 | ||||
| chr16:28494082-28494876 | Common:8; Rare:457 | ||||
| chr16:28538660-28539334 | Common:6; Rare:298 | ||||
| chr16:28553710-28554020 | Common:7; Rare:247 | ||||
| chr16:28553924-28554476 | Common:35; Rare:815 | ||||
| chr16:28596917-28597370 | Common:6; Rare:304 | ||||
| chr16:28609674-28610401 | Common:28; Rare:437 |