| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96399371-96399480 | Common:1; Rare:33 | ||||
| chr12:96400527-96400707 | Common:1; Rare:82 | ||||
| chr12:96907139-96907293 | Common:1; Rare:53 | ||||
| chr12:98515475-98515799 | Rare:105; Clinvar:2 | ||||
| chr12:98515833-98515882 | Rare:23; Clinvar (benign):1 | ||||
| chr12:98593474-98593776 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644731-98645296 | Common:5; Rare:162 | ||||
| chr12:100200707-100200846 | Rare:43 | ||||
| chr12:100267074-100267403 | Common:1; Rare:131 | ||||
| chr12:100573557-100573770 | Rare:73 | ||||
| chr12:101407663-101408056 | Common:3; Rare:98 | ||||
| chr12:101697805-101697948 | Rare:55 | ||||
| chr12:101877426-101877761 | Common:3; Rare:86 | ||||
| chr12:102120060-102120183 | Rare:46 | ||||
| chr12:103841019-103841476 | Common:6; Rare:141 |