| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11586891-11587058 | Common:2; Rare:46 | ||||
| chr16:11668264-11668530 | Common:3; Rare:120 | ||||
| chr16:11668766-11668775 | Rare:1 | ||||
| chr16:11742660-11743205 | Common:4; Rare:227 | ||||
| chr16:11796982-11797602 | Common:8; Rare:238 | ||||
| chr16:11797644-11797744 | Rare:32 | ||||
| chr16:11851189-11851315 | Common:3; Rare:29 | ||||
| chr16:11851429-11851701 | Common:1; Rare:143 | ||||
| chr16:11914991-11915020 | Rare:10 | ||||
| chr16:11915844-11916291 | Common:5; Rare:181 | ||||
| chr16:11976556-11976809 | Common:5; Rare:112 | ||||
| chr16:12803516-12803702 | Common:3; Rare:67 | ||||
| chr16:13919800-13920267 | Common:4; Rare:188; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:14071014-14071434 | Common:6; Rare:154 | ||||
| chr16:14501643-14501840 | Rare:36 |