| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11585927-11586297 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:11586812-11587314 | Common:4; Rare:123 | ||||
| chr16:11587338-11587475 | Rare:44 | ||||
| chr16:11668224-11668748 | Common:6; Rare:182 | ||||
| chr16:11742198-11742609 | Common:3; Rare:146 | ||||
| chr16:11742621-11743229 | Common:6; Rare:253 | ||||
| chr16:11796467-11796598 | Rare:35 | ||||
| chr16:11796935-11797277 | Common:6; Rare:134 | ||||
| chr16:11797279-11797626 | Common:2; Rare:125 | ||||
| chr16:11797684-11797723 | Rare:11 | ||||
| chr16:11797766-11797924 | Common:1; Rare:37 | ||||
| chr16:11850849-11851164 | Common:2; Rare:78 | ||||
| chr16:11851283-11851389 | Common:3; Rare:31 | ||||
| chr16:11851443-11851701 | Common:1; Rare:134 | ||||
| chr16:11914771-11914943 | Common:1; Rare:48 |