| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534332-6534578 | Common:5; Rare:106 | ||||
| chr12:6534654-6534851 | Common:3; Rare:82 | ||||
| chr12:6568241-6568369 | Rare:49 | ||||
| chr12:6851922-6852174 | Rare:63 | ||||
| chr12:6867342-6867612 | Common:2; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873282-6873526 | Common:2; Rare:72 | ||||
| chr12:6943875-6944161 | Common:10; Rare:294; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970616-6970961 | Common:3; Rare:108 | ||||
| chr12:7789231-7789452 | Common:2; Rare:44 | ||||
| chr12:8227579-8227691 | Rare:29 | ||||
| chr12:8914379-8914810 | Common:6; Rare:128 | ||||
| chr12:8949589-8949899 | Common:2; Rare:64 | ||||
| chr12:8949951-8950097 | Common:1; Rare:43 | ||||
| chr12:10613534-10613666 | Common:1; Rare:54 | ||||
| chr12:11171604-11171722 | Common:1; Rare:38 |