| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11976555-11976878 | Common:5; Rare:132 | ||||
| chr16:12803468-12803724 | Common:4; Rare:94 | ||||
| chr16:12803827-12804052 | Common:3; Rare:62 | ||||
| chr16:13919802-13920272 | Common:4; Rare:188; Clinvar:7; Clinvar (benign):1 | ||||
| chr16:14070980-14071109 | Common:2; Rare:46 | ||||
| chr16:14071228-14071466 | Common:3; Rare:90 | ||||
| chr16:14071708-14071779 | Common:1; Rare:13 | ||||
| chr16:14630058-14630531 | Rare:184 | ||||
| chr16:14632595-14633021 | Common:1; Rare:136 | ||||
| chr16:14633265-14633378 | Rare:38 | ||||
| chr16:14974568-14974688 | Rare:22 | ||||
| chr16:14974703-14975208 | Common:2; Rare:135 | ||||
| chr16:14975307-14975320 | Rare:1 | ||||
| chr16:15055715-15055871 | Rare:44 | ||||
| chr16:15055923-15056346 | Common:2; Rare:141 |