Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209637316-209637542 | Common:2; Rare:32 | ||||
chr1:209637700-209637984 | Common:1; Rare:69; Clinvar (benign):2 | ||||
chr1:209640577-209640651 | Rare:10 | ||||
chr1:209643820-209643956 | Common:1; Rare:18 | ||||
chr1:209653255-209653459 | Common:4; Rare:35 | ||||
chr1:209654149-209654235 | Rare:11 | ||||
chr1:209655880-209656077 | Rare:31 | ||||
chr1:209761012-209761045 | Rare:3 | ||||
chr1:209766045-209766349 | Common:2; Rare:56 | ||||
chr1:209771022-209771457 | Common:14; Rare:98 | ||||
chr1:209771867-209771996 | Common:2; Rare:18 | ||||
chr1:209772003-209772050 | Common:1; Rare:7 | ||||
chr1:209772059-209772418 | Rare:73 | ||||
chr1:209772422-209772598 | Rare:34 | ||||
chr1:209785298-209785361 | Rare:9 |