| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151697350-151697649 | Rare:112; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:152452542-152452690 | Common:1; Rare:22 | ||||
| chr2:160270293-160270623 | Common:2; Rare:80 | ||||
| chr2:169510607-169510896 | Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:170770764-170771048 | Common:1; Rare:48 | ||||
| chr2:178523094-178523239 | Rare:45 | ||||
| chr2:178545388-178546117 | Common:3; Rare:224; Clinvar:36; Clinvar (benign):21; Clinvar (pathogenic):3 | ||||
| chr2:178557647-178558639 | Common:3; Rare:286; Clinvar:34; Clinvar (benign):23; Clinvar (pathogenic):3 | ||||
| chr2:178577600-178578198 | Common:1; Rare:158; Clinvar:24; Clinvar (benign):11 | ||||
| chr2:178579559-178580230 | Common:4; Rare:183; Clinvar:25; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr2:178581497-178582209 | Common:2; Rare:207; Clinvar:35; Clinvar (benign):23; Clinvar (pathogenic):1 | ||||
| chr2:178582938-178583462 | Common:3; Rare:129; Clinvar:18; Clinvar (benign):11 | ||||
| chr2:178587115-178587820 | Common:2; Rare:207; Clinvar:31; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
| chr2:178591597-178592281 | Rare:198; Clinvar:33; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr2:178592377-178593084 | Common:2; Rare:192; Clinvar:28; Clinvar (benign):14; Clinvar (pathogenic):5 |