| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50685205-50685605 | Common:3; Rare:77 | ||||
| chr16:50694257-50694485 | Common:1; Rare:30 | ||||
| chr16:50694751-50696550 | Common:8; Rare:455 | ||||
| chr16:50698011-50698243 | Common:4; Rare:67 | ||||
| chr16:50698295-50698438 | Rare:28 | ||||
| chr16:50699810-50700200 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):6 | ||||
| chr16:50714928-50715091 | Rare:26 | ||||
| chr16:50735687-50736087 | Rare:117 | ||||
| chr16:50736544-50737041 | Rare:135 | ||||
| chr16:50740858-50741528 | Common:2; Rare:125 | ||||
| chr16:52577350-52577650 | Rare:66 | ||||
| chr16:53052623-53052848 | Rare:64 | ||||
| chr16:53052764-53053200 | Common:10; Rare:105 | ||||
| chr16:53055711-53055868 | Rare:27 | ||||
| chr16:53055918-53056891 | Common:2; Rare:198 |