| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752943-6753189 | Common:6; Rare:77 | ||||
| chr12:6766426-6766732 | Rare:83 | ||||
| chr12:6850984-6851054 | Rare:21 | ||||
| chr12:6851922-6852182 | Rare:66 | ||||
| chr12:6856095-6856372 | Rare:82 | ||||
| chr12:6867353-6867671 | Common:2; Rare:150; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873264-6873490 | Common:2; Rare:64 | ||||
| chr12:6943531-6943817 | Common:4; Rare:116 | ||||
| chr12:6943916-6944165 | Common:10; Rare:248; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970621-6970983 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr12:7018425-7018555 | Rare:41 | ||||
| chr12:7108375-7108608 | Common:2; Rare:78 | ||||
| chr12:7109132-7109429 | Common:1; Rare:85 | ||||
| chr12:7189544-7189731 | Rare:68; Clinvar:4 | ||||
| chr12:8032590-8032798 | Rare:71 |