| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54409620-54409857 | Rare:45 | ||||
| chr12:54414554-54414821 | Common:9; Rare:64 | ||||
| chr12:54416587-54416760 | Rare:28 | ||||
| chr12:54418066-54418237 | Rare:35 | ||||
| chr12:54428042-54428432 | Common:3; Rare:69 | ||||
| chr12:54428777-54428994 | Rare:33 | ||||
| chr12:55724600-55724857 | Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:55779714-55780052 | Common:1; Rare:58 | ||||
| chr12:55794856-55794949 | Rare:23 | ||||
| chr12:55819180-55819507 | Rare:106 | ||||
| chr12:55832147-55832360 | Rare:43 | ||||
| chr12:55861278-55861449 | Rare:28 | ||||
| chr12:55889843-55890104 | Common:2; Rare:36 | ||||
| chr12:55974660-55974911 | Common:1; Rare:34 | ||||
| chr12:56116021-56116071 | Rare:8 |