| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6873291-6873547 | Common:1; Rare:76 | ||||
| chr12:6943517-6943817 | Common:4; Rare:125 | ||||
| chr12:6943918-6944172 | Common:10; Rare:253; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944224-6944592 | Common:2; Rare:159; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:6970640-6970961 | Common:3; Rare:102 | ||||
| chr12:7108367-7108678 | Common:2; Rare:97 | ||||
| chr12:7109222-7109569 | Common:2; Rare:73 | ||||
| chr12:7189551-7189731 | Rare:66; Clinvar:4 | ||||
| chr12:8032489-8032793 | Common:5; Rare:91 | ||||
| chr12:8033507-8033716 | Rare:50 | ||||
| chr12:8066331-8066564 | Rare:33 | ||||
| chr12:8662628-8663041 | Common:4; Rare:92 | ||||
| chr12:8697731-8698029 | Common:1; Rare:118 | ||||
| chr12:8914374-8914723 | Common:6; Rare:101 | ||||
| chr12:8949583-8949862 | Common:1; Rare:57 |