| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2890628-2890946 | Common:2; Rare:227 | ||||
| chr12:2958986-2959519 | Common:5; Rare:273 | ||||
| chr12:2959785-2959984 | Common:3; Rare:92 | ||||
| chr12:3077206-3077438 | Common:13; Rare:172 | ||||
| chr12:4320941-4321260 | Common:10; Rare:239 | ||||
| chr12:4538425-4538959 | Common:6; Rare:247 | ||||
| chr12:4648966-4649225 | Common:3; Rare:125; Clinvar (benign):3 | ||||
| chr12:6200005-6200470 | Common:8; Rare:248 | ||||
| chr12:6341953-6342166 | Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6363240-6363490 | Common:3; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6364120-6364310 | Rare:43 | ||||
| chr12:6375909-6376309 | Common:2; Rare:87 | ||||
| chr12:6383961-6384301 | Common:3; Rare:123 | ||||
| chr12:6384740-6385440 | Common:6; Rare:226 | ||||
| chr12:6470632-6470875 | Common:2; Rare:129 |