| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50401104-50401202 | Rare:20 | ||||
| chr12:50401309-50401432 | Common:1; Rare:29 | ||||
| chr12:50763913-50764298 | Common:1; Rare:103 | ||||
| chr12:50924459-50924749 | Common:3; Rare:81 | ||||
| chr12:51009134-51009356 | Common:1; Rare:43 | ||||
| chr12:51026308-51026542 | Common:3; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048103-51048397 | Common:2; Rare:104 | ||||
| chr12:51173043-51173185 | Rare:27 | ||||
| chr12:51238658-51238914 | Common:8; Rare:114 | ||||
| chr12:51270278-51270532 | Common:5; Rare:65 | ||||
| chr12:51391407-51391464 | Rare:13 | ||||
| chr12:51391613-51391768 | Common:2; Rare:52 | ||||
| chr12:51907310-51907627 | Rare:75; Clinvar:3 | ||||
| chr12:51912210-51912425 | Common:1; Rare:49 | ||||
| chr12:52006680-52006946 | Rare:58 |