| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6319645-6319859 | Common:1; Rare:42 | ||||
| chr12:6330824-6331043 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6341580-6341755 | Common:1; Rare:47; Clinvar:1 | ||||
| chr12:6356311-6356473 | Rare:21 | ||||
| chr12:6356666-6356893 | Common:3; Rare:39 | ||||
| chr12:6361972-6362166 | Rare:73; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:6362178-6362349 | Rare:50; Clinvar:1 | ||||
| chr12:6363550-6363971 | Common:4; Rare:132; Clinvar (benign):2 | ||||
| chr12:6374689-6375172 | Common:3; Rare:160; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:6375261-6375668 | Common:5; Rare:102; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376212-6376414 | Common:2; Rare:40 | ||||
| chr12:6383976-6384250 | Common:1; Rare:63 | ||||
| chr12:6451785-6452184 | Common:4; Rare:76 | ||||
| chr12:6470643-6470902 | Common:2; Rare:72 | ||||
| chr12:6493088-6493381 | Common:7; Rare:87 |