Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209827814-209828086 | Common:2; Rare:71 | ||||
chr1:209937970-209938257 | Common:3; Rare:94; Clinvar (pathogenic):1 | ||||
chr1:211259029-211259400 | Common:1; Rare:113 | ||||
chr1:211259733-211259980 | Rare:69 | ||||
chr1:211326698-211326892 | Common:3; Rare:51 | ||||
chr1:211579034-211579269 | Rare:62 | ||||
chr1:211675531-211675769 | Rare:50 | ||||
chr1:212035488-212035810 | Common:2; Rare:90 | ||||
chr1:212285081-212285556 | Common:3; Rare:148 | ||||
chr1:212286023-212286147 | Common:1; Rare:40 | ||||
chr1:212414724-212415023 | Common:3; Rare:104 | ||||
chr1:212432769-212432956 | Rare:57 | ||||
chr1:212608488-212608762 | Rare:69 | ||||
chr1:212791716-212791982 | Common:6; Rare:127 | ||||
chr1:212858037-212858455 | Common:6; Rare:113; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |