| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3500849-3501065 | Common:3; Rare:82 | ||||
| chr16:3611567-3611803 | Rare:103; Clinvar:1 | ||||
| chr16:4425769-4425892 | Common:1; Rare:59 | ||||
| chr16:4476273-4476466 | Common:3; Rare:72 | ||||
| chr16:4538394-4538607 | Common:2; Rare:73 | ||||
| chr16:4614886-4615138 | Common:1; Rare:76 | ||||
| chr16:4734199-4734534 | Common:1; Rare:109 | ||||
| chr16:5033926-5033967 | Rare:13 | ||||
| chr16:5097737-5098007 | Common:4; Rare:98 | ||||
| chr16:8797612-8797885 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868983-8869242 | Common:4; Rare:116 | ||||
| chr16:11586891-11587034 | Common:1; Rare:43 | ||||
| chr16:11587161-11587313 | Common:1; Rare:35 | ||||
| chr16:11851499-11851635 | Rare:67 | ||||
| chr16:11915883-11916269 | Common:2; Rare:157 |