| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867409-6867616 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873327-6873546 | Common:1; Rare:61 | ||||
| chr12:6904676-6905041 | Common:2; Rare:82 | ||||
| chr12:6914385-6914659 | Common:2; Rare:70 | ||||
| chr12:6943517-6943826 | Common:4; Rare:135 | ||||
| chr12:6943926-6944130 | Common:8; Rare:209; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:6970612-6970961 | Common:3; Rare:109 | ||||
| chr12:7018468-7018584 | Common:1; Rare:30 | ||||
| chr12:7130053-7130423 | Common:6; Rare:88 | ||||
| chr12:7189519-7189733 | Rare:73; Clinvar:4 | ||||
| chr12:8697762-8698124 | Common:3; Rare:127 | ||||
| chr12:8914368-8914735 | Common:6; Rare:106 | ||||
| chr12:8949574-8949852 | Common:1; Rare:57 | ||||
| chr12:8949960-8950119 | Common:1; Rare:41 | ||||
| chr12:9115803-9116207 | Common:3; Rare:87 |