| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493230-6493394 | Common:6; Rare:46 | ||||
| chr12:6493793-6494140 | Common:2; Rare:104 | ||||
| chr12:6549089-6549258 | Common:1; Rare:32 | ||||
| chr12:6568244-6568382 | Rare:52 | ||||
| chr12:6591483-6591696 | Rare:54 | ||||
| chr12:6689490-6689748 | Common:1; Rare:60 | ||||
| chr12:6723847-6724176 | Common:1; Rare:70 | ||||
| chr12:6724196-6724306 | Common:1; Rare:25 | ||||
| chr12:6766510-6766747 | Rare:64 | ||||
| chr12:6829644-6829768 | Common:1; Rare:21 | ||||
| chr12:6851239-6851492 | Rare:60 | ||||
| chr12:6851922-6852203 | Rare:73 | ||||
| chr12:6873257-6873541 | Common:2; Rare:84 | ||||
| chr12:6943926-6944172 | Common:8; Rare:246; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970557-6970988 | Common:4; Rare:139; Clinvar (benign):1 |