| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123419869-123420062 | Rare:30 | ||||
| chr12:6226068-6226331 | Common:1; Rare:45 | ||||
| chr12:6962970-6963240 | Common:1; Rare:50 | ||||
| chr12:8242916-8243226 | Common:8; Rare:95 | ||||
| chr12:9911017-9911305 | Common:3; Rare:72 | ||||
| chr12:56634991-56635243 | Common:1; Rare:41 | ||||
| chr12:120291901-120292196 | Common:8; Rare:116 | ||||
| chr12:127205742-127205897 | Rare:32 | ||||
| chr13:27969123-27969485 | Rare:80 | ||||
| chr13:29140329-29140560 | Rare:37 | ||||
| chr13:48413111-48413208 | Rare:13 | ||||
| chr14:40629807-40630028 | Common:4; Rare:86 | ||||
| chr14:49633956-49634047 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862713-49862969 | Rare:122 | ||||
| chr14:55127609-55127877 | Common:2; Rare:43 |