| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6943897-6944172 | Common:10; Rare:277; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970624-6970983 | Common:4; Rare:118; Clinvar (benign):1 | ||||
| chr12:7018414-7018587 | Common:1; Rare:50 | ||||
| chr12:7060423-7060874 | Rare:88 | ||||
| chr12:7108334-7108696 | Common:2; Rare:110 | ||||
| chr12:7189526-7189731 | Rare:70; Clinvar:4 | ||||
| chr12:8032589-8032793 | Rare:71 | ||||
| chr12:8662631-8662937 | Common:4; Rare:66 | ||||
| chr12:8697837-8698019 | Rare:72 | ||||
| chr12:8914396-8914714 | Common:6; Rare:97 | ||||
| chr12:9869352-9869587 | Common:3; Rare:38 | ||||
| chr12:10212839-10212937 | Rare:26 | ||||
| chr12:10613508-10613686 | Common:1; Rare:70 | ||||
| chr12:11171587-11171638 | Rare:17 | ||||
| chr12:12357004-12357131 | Common:1; Rare:66 |