| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752938-6753201 | Common:6; Rare:85 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6867358-6867611 | Common:2; Rare:125; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873655 | Common:3; Rare:107 | ||||
| chr12:6904676-6905037 | Common:2; Rare:80 | ||||
| chr12:6927584-6927813 | Rare:58 | ||||
| chr12:6943531-6943829 | Common:4; Rare:129 | ||||
| chr12:6943915-6944172 | Common:10; Rare:256; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970621-6970988 | Common:4; Rare:121; Clinvar (benign):1 | ||||
| chr12:7018431-7018584 | Common:1; Rare:46 | ||||
| chr12:7060338-7060550 | Rare:52 | ||||
| chr12:7061480-7061607 | Rare:22 | ||||
| chr12:7091762-7092005 | Common:1; Rare:64 | ||||
| chr12:7092387-7092672 | Rare:66 | ||||
| chr12:7108442-7108696 | Common:1; Rare:73 |