| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534724-6534858 | Common:2; Rare:60 | ||||
| chr12:6568260-6568354 | Rare:35 | ||||
| chr12:6723849-6724178 | Common:1; Rare:70 | ||||
| chr12:6752934-6753189 | Common:6; Rare:78 | ||||
| chr12:6873282-6873483 | Common:2; Rare:57 | ||||
| chr12:6943760-6944172 | Common:16; Rare:417; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970380-6971080 | Common:10; Rare:221; Clinvar (benign):2 | ||||
| chr12:7108448-7108697 | Common:1; Rare:71 | ||||
| chr12:10172093-10172261 | Rare:43 | ||||
| chr12:11171600-11171711 | Common:1; Rare:36 | ||||
| chr12:12357001-12357129 | Common:1; Rare:68 | ||||
| chr12:12717350-12717393 | Rare:17 | ||||
| chr12:12891684-12891953 | Common:4; Rare:45 | ||||
| chr12:14365492-14365688 | Common:1; Rare:61 | ||||
| chr12:14567719-14567922 | Common:1; Rare:38 |