| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104138147-104138432 | Common:1; Rare:80 | ||||
| chr12:104287173-104287219 | Rare:6 | ||||
| chr12:104958196-104958380 | Common:3; Rare:54 | ||||
| chr12:104986182-104986353 | Common:3; Rare:56 | ||||
| chr12:105107605-105107806 | Common:1; Rare:94; Clinvar:1 | ||||
| chr12:105236029-105236374 | Common:3; Rare:151 | ||||
| chr12:106247502-106247721 | Common:4; Rare:86 | ||||
| chr12:106302730-106302866 | Common:4; Rare:42 | ||||
| chr12:106357434-106357823 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357939-106358111 | Common:3; Rare:79 | ||||
| chr12:106774103-106774730 | Common:5; Rare:165 | ||||
| chr12:106774856-106774942 | Rare:38 | ||||
| chr12:106955436-106955907 | Common:3; Rare:178 | ||||
| chr12:107093503-107093602 | Rare:39 | ||||
| chr12:107685695-107685939 | Rare:79 |