| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201116632-201116890 | Rare:92 | ||||
| chr2:201117030-201117290 | Rare:74 | ||||
| chr2:201117422-201117619 | Rare:40 | ||||
| chr2:201118480-201118854 | Rare:90 | ||||
| chr2:201182967-201183167 | Common:1; Rare:30; Clinvar (benign):2 | ||||
| chr2:201233321-201233587 | Common:2; Rare:79 | ||||
| chr2:201257712-201258118 | Common:2; Rare:135 | ||||
| chr2:201258161-201258357 | Common:4; Rare:107; Clinvar (benign):4 | ||||
| chr2:201451391-201451826 | Common:3; Rare:213 | ||||
| chr2:201642633-201642785 | Rare:128 | ||||
| chr2:201780881-201780984 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238511-202238640 | Rare:86 | ||||
| chr2:202265618-202266014 | Common:2; Rare:201 | ||||
| chr2:202376074-202376521 | Rare:157 | ||||
| chr2:202376920-202377310 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):5 |