| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49758223-49758476 | Common:4; Rare:79 | ||||
| chr12:49828374-49828543 | Common:1; Rare:64 | ||||
| chr12:49843092-49843172 | Rare:27 | ||||
| chr12:50085275-50085364 | Common:1; Rare:22 | ||||
| chr12:50167288-50167672 | Common:3; Rare:106 | ||||
| chr12:50283440-50283656 | Common:1; Rare:68 | ||||
| chr12:50400714-50400973 | Rare:79 | ||||
| chr12:50504832-50505111 | Common:3; Rare:113 | ||||
| chr12:50763913-50764326 | Common:1; Rare:112 | ||||
| chr12:51026321-51026608 | Common:6; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048174-51048359 | Common:1; Rare:71 | ||||
| chr12:51172765-51172874 | Common:1; Rare:23 | ||||
| chr12:51173081-51173235 | Rare:27 | ||||
| chr12:51238658-51238899 | Common:8; Rare:110 | ||||
| chr12:51239121-51239319 | Common:2; Rare:57 |