| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:131911379-131911460 | Common:1; Rare:36 | ||||
| chr11:134253298-134253592 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr12:389249-389347 | Rare:38 | ||||
| chr12:2004430-2004723 | Common:2; Rare:88 | ||||
| chr12:2877031-2877262 | Rare:70 | ||||
| chr12:3077267-3077406 | Common:4; Rare:59 | ||||
| chr12:4321064-4321258 | Common:4; Rare:71 | ||||
| chr12:4538497-4538930 | Common:3; Rare:94 | ||||
| chr12:4648998-4649149 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr12:6341989-6342394 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6375380-6375667 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6383988-6384225 | Common:1; Rare:54 | ||||
| chr12:6493230-6493386 | Common:6; Rare:44 | ||||
| chr12:6493783-6494138 | Common:2; Rare:107 | ||||
| chr12:6534335-6534582 | Common:5; Rare:109 |