| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95943206-95943425 | Common:2; Rare:42 | ||||
| chr12:95996230-95996589 | Common:4; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96907197-96907293 | Rare:37 | ||||
| chr12:98515435-98515702 | Rare:86; Clinvar:1 | ||||
| chr12:98515833-98515951 | Rare:40; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:98644997-98645317 | Common:2; Rare:97 | ||||
| chr12:100267047-100267312 | Common:1; Rare:119 | ||||
| chr12:101280019-101280143 | Common:1; Rare:40 | ||||
| chr12:101407641-101408056 | Common:3; Rare:105 | ||||
| chr12:101877447-101877778 | Common:4; Rare:90 | ||||
| chr12:102120065-102120223 | Rare:60 | ||||
| chr12:102478551-102478653 | Rare:19 | ||||
| chr12:102480458-102480714 | Rare:29 | ||||
| chr12:102915213-102915303 | Common:1; Rare:14 | ||||
| chr12:102917074-102917423 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 |