| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6904678-6904985 | Common:4; Rare:174 | ||||
| chr12:6905356-6905710 | Common:3; Rare:75 | ||||
| chr12:6914230-6914650 | Common:1; Rare:220 | ||||
| chr12:6927572-6927895 | Rare:190 | ||||
| chr12:6927850-6928363 | Common:5; Rare:256 | ||||
| chr12:6928601-6929001 | Rare:75 | ||||
| chr12:6937956-6938278 | Common:1; Rare:231; Clinvar (benign):1 | ||||
| chr12:6943489-6944194 | Common:44; Rare:1271; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6946209-6946763 | Common:6; Rare:395 | ||||
| chr12:6970484-6971092 | Common:22; Rare:510; Clinvar (benign):5 | ||||
| chr12:6988294-6988469 | Common:1; Rare:32 | ||||
| chr12:7018422-7019061 | Common:7; Rare:303 | ||||
| chr12:7129995-7130172 | Common:1; Rare:42 | ||||
| chr12:7130240-7130432 | Common:14; Rare:141 | ||||
| chr12:7155440-7155960 | Common:3; Rare:162 |