| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864568-200864788 | Common:1; Rare:81 | ||||
| chr2:200889037-200889439 | Common:3; Rare:130 | ||||
| chr2:200963588-200963903 | Common:1; Rare:82 | ||||
| chr2:201071620-201072047 | Rare:89 | ||||
| chr2:201115949-201116034 | Rare:14 | ||||
| chr2:201116105-201116454 | Common:1; Rare:65 | ||||
| chr2:201118365-201118831 | Rare:71 | ||||
| chr2:201451416-201451826 | Common:2; Rare:110 | ||||
| chr2:201642637-201642743 | Rare:53 | ||||
| chr2:202238443-202238615 | Rare:60; Clinvar:1 | ||||
| chr2:202265623-202265808 | Rare:68 | ||||
| chr2:202376420-202376609 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:202377072-202377372 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chr2:202911606-202912013 | Common:1; Rare:84 | ||||
| chr2:202912140-202912298 | Common:2; Rare:54 |