Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26692458-26692847 | Common:2; Rare:96 | ||||
chr2:26764183-26764347 | Common:2; Rare:65 | ||||
chr2:26847977-26848249 | Rare:80 | ||||
chr2:26970325-26970733 | Rare:109 | ||||
chr2:27032808-27033041 | Rare:87 | ||||
chr2:27051539-27051748 | Rare:65 | ||||
chr2:27071545-27071888 | Common:1; Rare:103 | ||||
chr2:27086532-27086773 | Common:3; Rare:76 | ||||
chr2:27134582-27134728 | Rare:69 | ||||
chr2:27211712-27212192 | Common:4; Rare:165 | ||||
chr2:27212223-27212384 | Common:2; Rare:85 | ||||
chr2:27212771-27212836 | Rare:10 | ||||
chr2:27217304-27217535 | Rare:99 | ||||
chr2:27323045-27323154 | Rare:26; Clinvar (benign):1 | ||||
chr2:27356750-27357191 | Common:2; Rare:132 |