| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73071322-73071485 | Common:1; Rare:52 | ||||
| chr2:73071689-73071870 | Common:2; Rare:72 | ||||
| chr2:73214193-73214616 | Common:5; Rare:163 | ||||
| chr2:73214624-73214710 | Rare:25 | ||||
| chr2:73232986-73233152 | Rare:32 | ||||
| chr2:73233168-73233504 | Common:2; Rare:101 | ||||
| chr2:73233671-73233690 | Rare:2 | ||||
| chr2:73233915-73234361 | Common:4; Rare:97 | ||||
| chr2:73234550-73234582 | Rare:10 | ||||
| chr2:73385599-73386116 | Common:4; Rare:237; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr2:73386212-73386326 | Rare:44 | ||||
| chr2:73736755-73736853 | Common:1; Rare:19 | ||||
| chr2:73737228-73737553 | Common:3; Rare:106 | ||||
| chr2:73828804-73829041 | Common:1; Rare:56 | ||||
| chr2:73926781-73926933 | Common:1; Rare:87; Clinvar:7; Clinvar (benign):3 |