| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392651-177393059 | Common:3; Rare:141; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552750-177552838 | Common:1; Rare:32 | ||||
| chr2:177618703-177619023 | Common:7; Rare:90 | ||||
| chr2:178072738-178072863 | Rare:35 | ||||
| chr2:178450713-178450940 | Common:1; Rare:90 | ||||
| chr2:178451083-178451310 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478504-178478659 | Common:1; Rare:47 | ||||
| chr2:180980279-180980545 | Common:1; Rare:86 | ||||
| chr2:180980872-180981225 | Rare:89 | ||||
| chr2:181680397-181680846 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:182427007-182427106 | Rare:18 | ||||
| chr2:182522391-182522688 | Common:2; Rare:55 | ||||
| chr2:182522692-182522855 | Common:1; Rare:32 | ||||
| chr2:182716169-182716399 | Common:2; Rare:74 | ||||
| chr2:183078680-183078792 | Rare:20 |