| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:680217-680544 | Common:3; Rare:101 | ||||
| chr16:684242-684509 | Common:3; Rare:142 | ||||
| chr16:690067-690225 | Common:1; Rare:41 | ||||
| chr16:690290-690544 | Common:3; Rare:103 | ||||
| chr16:720493-720705 | Common:1; Rare:52 | ||||
| chr16:721020-721178 | Common:2; Rare:41 | ||||
| chr16:721277-721544 | Common:3; Rare:101 | ||||
| chr16:740881-741219 | Common:3; Rare:110 | ||||
| chr16:788310-788765 | Common:4; Rare:230 | ||||
| chr16:970452-970582 | Rare:39 | ||||
| chr16:970887-971222 | Common:6; Rare:143 | ||||
| chr16:981168-981453 | Common:17; Rare:148 | ||||
| chr16:981509-981805 | Common:4; Rare:100 | ||||
| chr16:1152974-1153154 | Common:2; Rare:72 | ||||
| chr16:1153975-1154038 | Common:1; Rare:18; Clinvar (benign):1 |