| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224530-134224667 | Rare:49 | ||||
| chr11:134253286-134253586 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr12:389238-389399 | Common:1; Rare:62 | ||||
| chr12:401446-401645 | Rare:53 | ||||
| chr12:643624-643657 | Rare:5 | ||||
| chr12:752306-752602 | Common:1; Rare:88 | ||||
| chr12:990765-990873 | Rare:31 | ||||
| chr12:991101-991316 | Common:3; Rare:98 | ||||
| chr12:2004345-2004629 | Common:1; Rare:111 | ||||
| chr12:2798927-2799155 | Rare:53 | ||||
| chr12:2877039-2877262 | Rare:67 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4275448-4275691 | Common:3; Rare:41 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538487-4538930 | Common:3; Rare:96 |