| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8674419-8674673 | Common:1; Rare:88; Clinvar:2 | ||||
| chr16:8797625-8797889 | Rare:103; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868983-8869274 | Common:4; Rare:128 | ||||
| chr16:8896997-8897310 | Rare:82 | ||||
| chr16:10580569-10580702 | Rare:43 | ||||
| chr16:10580825-10580858 | Rare:10 | ||||
| chr16:10744061-10744306 | Common:1; Rare:90 | ||||
| chr16:10944327-10944638 | Common:1; Rare:97 | ||||
| chr16:11586891-11587036 | Common:1; Rare:44 | ||||
| chr16:11587172-11587310 | Common:1; Rare:33 | ||||
| chr16:11742853-11743134 | Common:3; Rare:116 | ||||
| chr16:11797180-11797545 | Common:4; Rare:143 | ||||
| chr16:11851508-11851652 | Rare:69 | ||||
| chr16:11886916-11887075 | Common:1; Rare:44 | ||||
| chr16:11915380-11915727 | Common:5; Rare:133 |