| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178621473-178622012 | Common:4; Rare:149; Clinvar:18; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
| chr2:178625271-178625603 | Common:1; Rare:74; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:178630802-178631303 | Common:1; Rare:120; Clinvar:20; Clinvar (benign):8 | ||||
| chr2:178688109-178688372 | Common:1; Rare:48; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:178689513-178689915 | Common:2; Rare:97; Clinvar:9; Clinvar (benign):11 | ||||
| chr2:178704875-178705358 | Rare:102; Clinvar:9; Clinvar (benign):6 | ||||
| chr2:178718793-178719239 | Common:1; Rare:115; Clinvar:9; Clinvar (benign):9 | ||||
| chr2:178719981-178720665 | Common:2; Rare:183; Clinvar:18; Clinvar (benign):14 | ||||
| chr2:178723044-178723670 | Rare:181; Clinvar:35; Clinvar (benign):11 | ||||
| chr2:178769678-178770320 | Common:3; Rare:147; Clinvar:15; Clinvar (benign):13 | ||||
| chr2:178773836-178774476 | Common:1; Rare:194; Clinvar:32; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr2:178804537-178804835 | Rare:77; Clinvar:6; Clinvar (benign):7 | ||||
| chr2:191846453-191846731 | Common:4; Rare:100 | ||||
| chr2:200416327-200416417 | Rare:10 | ||||
| chr2:202376111-202376219 | Rare:65 |