| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071698-5071852 | Rare:69; Clinvar (benign):1 | ||||
| chr16:5097737-5098025 | Common:4; Rare:100 | ||||
| chr16:8797610-8797866 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868983-8869261 | Common:4; Rare:123 | ||||
| chr16:11668281-11668517 | Common:3; Rare:104 | ||||
| chr16:11851507-11851635 | Rare:61 | ||||
| chr16:11915380-11915727 | Common:5; Rare:133 | ||||
| chr16:11915889-11916208 | Common:2; Rare:131 | ||||
| chr16:11976610-11976769 | Common:3; Rare:62 | ||||
| chr16:12803800-12803976 | Common:2; Rare:49 | ||||
| chr16:14071048-14071368 | Common:4; Rare:111 | ||||
| chr16:14630188-14630484 | Rare:116 | ||||
| chr16:14632729-14632995 | Common:1; Rare:89 | ||||
| chr16:15094226-15094409 | Common:1; Rare:92 | ||||
| chr16:15643037-15643286 | Common:1; Rare:85; Clinvar:1 |