Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:56854660-56854983 | Common:3; Rare:67 | ||||
chr1:56965862-56966230 | Common:2; Rare:86 | ||||
chr1:58783991-58784257 | Rare:64 | ||||
chr1:59296512-59296842 | Common:12; Rare:88 | ||||
chr1:59926712-59927110 | Common:2; Rare:94 | ||||
chr1:61082084-61082132 | Rare:9 | ||||
chr1:62597462-62598080 | Common:2; Rare:164; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr1:62600896-62601196 | Common:2; Rare:61 | ||||
chr1:62688256-62688545 | Common:1; Rare:109; Clinvar:1 | ||||
chr1:62784081-62784180 | Rare:43 | ||||
chr1:63523186-63523581 | Common:3; Rare:100 | ||||
chr1:63592887-63593582 | Rare:196; Clinvar (benign):3 | ||||
chr1:63593677-63593736 | Rare:27 | ||||
chr1:64841243-64841541 | Rare:69; Clinvar:2 | ||||
chr1:65147281-65147659 | Rare:97 |