| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6724220-6724291 | Rare:13 | ||||
| chr12:6752932-6753205 | Common:6; Rare:86 | ||||
| chr12:6851887-6852179 | Rare:76 | ||||
| chr12:6867358-6867594 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869445-6869714 | Common:1; Rare:75 | ||||
| chr12:6873282-6873541 | Common:2; Rare:74 | ||||
| chr12:6943531-6943834 | Common:4; Rare:135 | ||||
| chr12:6943926-6944172 | Common:8; Rare:246; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970602-6970961 | Common:3; Rare:111 | ||||
| chr12:7060392-7060876 | Rare:96 | ||||
| chr12:7064049-7064290 | Common:1; Rare:64 | ||||
| chr12:7090190-7090430 | Common:4; Rare:55; Clinvar:1 | ||||
| chr12:7091867-7091920 | Rare:9 | ||||
| chr12:7108442-7108681 | Common:1; Rare:71 | ||||
| chr12:7109105-7109315 | Rare:66 |