| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2877033-2877262 | Rare:69 | ||||
| chr12:2959833-2959897 | Rare:16 | ||||
| chr12:4275452-4275564 | Common:2; Rare:14 | ||||
| chr12:4320934-4321258 | Common:5; Rare:124 | ||||
| chr12:4538444-4538736 | Rare:61 | ||||
| chr12:4649026-4649154 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr12:6200005-6200480 | Common:4; Rare:138 | ||||
| chr12:6375432-6375462 | Rare:4 | ||||
| chr12:6493240-6493386 | Common:5; Rare:41 | ||||
| chr12:6493789-6494001 | Common:2; Rare:74 | ||||
| chr12:6568260-6568382 | Rare:46 | ||||
| chr12:6752949-6753173 | Common:6; Rare:67 | ||||
| chr12:6851879-6852180 | Rare:81 | ||||
| chr12:6867428-6867555 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6943979-6944172 | Common:3; Rare:189; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 |