| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2877009-2877287 | Rare:94 | ||||
| chr12:2890692-2890938 | Common:1; Rare:99 | ||||
| chr12:2958895-2959028 | Common:2; Rare:35 | ||||
| chr12:2959795-2959958 | Common:1; Rare:42 | ||||
| chr12:3077267-3077412 | Common:5; Rare:62 | ||||
| chr12:3753064-3753267 | Common:2; Rare:48 | ||||
| chr12:3873348-3873580 | Common:2; Rare:56 | ||||
| chr12:4320947-4321260 | Common:5; Rare:118 | ||||
| chr12:4538440-4538942 | Common:3; Rare:113 | ||||
| chr12:4604807-4605023 | Common:4; Rare:79 | ||||
| chr12:4649011-4649178 | Common:2; Rare:56; Clinvar (benign):2 | ||||
| chr12:6200233-6200471 | Common:3; Rare:73 | ||||
| chr12:6341841-6342185 | Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6375382-6375429 | Rare:5 | ||||
| chr12:6383988-6384250 | Common:1; Rare:57 |