| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253290-134253586 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr12:389249-389358 | Rare:39 | ||||
| chr12:2004420-2004668 | Common:2; Rare:80 | ||||
| chr12:2877031-2877262 | Rare:70 | ||||
| chr12:4320949-4321253 | Common:5; Rare:115 | ||||
| chr12:4538501-4538784 | Rare:56 | ||||
| chr12:4649026-4649143 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr12:6200005-6200446 | Common:4; Rare:126 | ||||
| chr12:6375426-6375537 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6383976-6384234 | Common:1; Rare:61 | ||||
| chr12:6493240-6493377 | Common:5; Rare:38 | ||||
| chr12:6493782-6494140 | Common:2; Rare:107 | ||||
| chr12:6568255-6568393 | Rare:54 | ||||
| chr12:6663102-6663402 | Common:2; Rare:83 | ||||
| chr12:6723848-6724074 | Common:1; Rare:38 |