| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828381-49828543 | Common:1; Rare:59 | ||||
| chr12:49843058-49843187 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr12:50167279-50167717 | Common:3; Rare:117 | ||||
| chr12:50222477-50222502 | Rare:7 | ||||
| chr12:50283470-50283675 | Common:3; Rare:67 | ||||
| chr12:50763927-50764297 | Common:1; Rare:97 | ||||
| chr12:51239133-51239338 | Common:2; Rare:60 | ||||
| chr12:51269938-51270059 | Rare:54 | ||||
| chr12:51270417-51270717 | Common:5; Rare:68 | ||||
| chr12:51391321-51391460 | Common:2; Rare:32 | ||||
| chr12:52006703-52006946 | Rare:49 | ||||
| chr12:52948824-52949159 | Common:2; Rare:82 | ||||
| chr12:52949725-52950028 | Rare:71 | ||||
| chr12:53047058-53047264 | Common:1; Rare:48 | ||||
| chr12:53079333-53079537 | Common:2; Rare:71 |