| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178652641-178652941 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):7 | ||||
| chr2:178654255-178654453 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:178678392-178678834 | Common:1; Rare:98; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr2:178679869-178680334 | Common:1; Rare:118; Clinvar:13; Clinvar (benign):4 | ||||
| chr2:178681077-178681454 | Common:1; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:178682688-178683302 | Common:4; Rare:128; Clinvar:17; Clinvar (benign):7 | ||||
| chr2:178683981-178684423 | Common:5; Rare:100; Clinvar:13; Clinvar (benign):9 | ||||
| chr2:178684664-178684995 | Rare:92; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:178688644-178689155 | Common:2; Rare:148; Clinvar:12; Clinvar (benign):10 | ||||
| chr2:178689501-178689906 | Common:2; Rare:99; Clinvar:9; Clinvar (benign):11 | ||||
| chr2:178701495-178701612 | Rare:35; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:178704846-178705358 | Rare:107; Clinvar:9; Clinvar (benign):6 | ||||
| chr2:178711942-178712596 | Rare:196; Clinvar:24; Clinvar (benign):17 | ||||
| chr2:178718320-178718975 | Common:3; Rare:187; Clinvar:30; Clinvar (benign):17 | ||||
| chr2:178723044-178723712 | Rare:192; Clinvar:38; Clinvar (benign):12 |