| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32010751-32010890 | Common:1; Rare:38 | ||||
| chr2:32010919-32011187 | Rare:80 | ||||
| chr2:32039436-32039644 | Rare:59 | ||||
| chr2:32039740-32039938 | Rare:64 | ||||
| chr2:32040086-32040170 | Rare:17 | ||||
| chr2:32063103-32063153 | Rare:14 | ||||
| chr2:32063315-32063804 | Common:2; Rare:171; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:32063809-32064022 | Common:1; Rare:108; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:32064047-32064110 | Rare:22 | ||||
| chr2:32064136-32064209 | Rare:29; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:32165438-32165485 | Rare:10 | ||||
| chr2:32165607-32166017 | Common:3; Rare:159 | ||||
| chr2:32277717-32277989 | Common:1; Rare:64 | ||||
| chr2:32278087-32278268 | Rare:62 | ||||
| chr2:32278347-32278432 | Rare:18 |