| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6828359-6828419 | Common:2; Rare:8 | ||||
| chr12:6851245-6851461 | Rare:50 | ||||
| chr12:6851922-6852203 | Rare:73 | ||||
| chr12:6873274-6873479 | Common:2; Rare:59 | ||||
| chr12:6927548-6927818 | Rare:67 | ||||
| chr12:6943926-6944173 | Common:8; Rare:247; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970570-6970988 | Common:4; Rare:134; Clinvar (benign):1 | ||||
| chr12:7060388-7060867 | Rare:96 | ||||
| chr12:7108442-7108722 | Common:1; Rare:77 | ||||
| chr12:10172113-10172261 | Rare:36 | ||||
| chr12:10613528-10613703 | Common:1; Rare:70 | ||||
| chr12:11170950-11171261 | Common:4; Rare:89 | ||||
| chr12:11171551-11171728 | Common:2; Rare:60 | ||||
| chr12:12356986-12357178 | Common:4; Rare:102 | ||||
| chr12:12611769-12612074 | Common:2; Rare:88 |