| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177212102-177212846 | Common:7; Rare:249 | ||||
| chr2:177213118-177213230 | Rare:55 | ||||
| chr2:177263484-177263771 | Common:2; Rare:74 | ||||
| chr2:177263828-177263979 | Common:2; Rare:32 | ||||
| chr2:177263982-177264442 | Rare:131 | ||||
| chr2:177264621-177265420 | Common:7; Rare:194 | ||||
| chr2:177265451-177265556 | Rare:22 | ||||
| chr2:177392490-177392828 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:177392850-177392984 | Common:1; Rare:45; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:177552635-177553179 | Common:5; Rare:188 | ||||
| chr2:177618628-177618787 | Common:1; Rare:81 | ||||
| chr2:177618869-177619079 | Common:3; Rare:61 | ||||
| chr2:178112264-178112654 | Common:2; Rare:122 | ||||
| chr2:178450471-178450594 | Common:1; Rare:30 | ||||
| chr2:178450634-178450964 | Common:1; Rare:129; Clinvar:1 |