| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867263-6867671 | Common:10; Rare:613; Clinvar:8; Clinvar (benign):10 | ||||
| chr12:6867891-6868291 | Common:15; Rare:224 | ||||
| chr12:6868586-6869393 | Common:4; Rare:960; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):14 | ||||
| chr12:6870098-6871139 | Common:9; Rare:463; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:6873221-6873683 | Common:17; Rare:594 | ||||
| chr12:6904555-6904955 | Common:5; Rare:325 | ||||
| chr12:6914293-6915265 | Common:7; Rare:321 | ||||
| chr12:6915264-6915856 | Common:9; Rare:285 | ||||
| chr12:6924160-6924620 | Common:2; Rare:93 | ||||
| chr12:6927446-6928664 | Common:14; Rare:937 | ||||
| chr12:6937845-6938340 | Common:5; Rare:558; Clinvar (benign):4 | ||||
| chr12:6942774-6943009 | Common:3; Rare:96 | ||||
| chr12:6943330-6943830 | Common:18; Rare:734 | ||||
| chr12:6943803-6944816 | Common:68; Rare:2293; Clinvar:51; Clinvar (benign):16; Clinvar (pathogenic):12 | ||||
| chr12:6946240-6946693 | Common:5; Rare:425 |