| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47865078-47865427 | Common:2; Rare:95; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr12:49028879-49029086 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr12:49060761-49060876 | Common:1; Rare:47 | ||||
| chr12:50106014-50106332 | Common:3; Rare:62 | ||||
| chr12:51240189-51240399 | Rare:41 | ||||
| chr12:52052034-52052145 | Common:2; Rare:17 | ||||
| chr12:52082082-52082166 | Common:2; Rare:19 | ||||
| chr12:53051641-53051936 | Rare:66 | ||||
| chr12:55833960-55833973 | Rare:5 | ||||
| chr12:56080812-56080825 | Rare:1 | ||||
| chr12:56170181-56170361 | Common:3; Rare:52 | ||||
| chr12:56190239-56190322 | Common:1; Rare:43 | ||||
| chr12:56234882-56235196 | Common:1; Rare:106 | ||||
| chr12:56235642-56235946 | Common:4; Rare:98; Clinvar (pathogenic):1 | ||||
| chr12:56634966-56635116 | Common:1; Rare:27 |