Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593060-63593520 | Rare:140; Clinvar (benign):2 | ||||
chr1:63593540-63593950 | Common:3; Rare:178; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:63594236-63594555 | Common:3; Rare:69 | ||||
chr1:63773889-63774038 | Rare:27 | ||||
chr1:64744827-64745068 | Rare:77 | ||||
chr1:64966478-64966724 | Common:1; Rare:94 | ||||
chr1:65147540-65147643 | Rare:30 | ||||
chr1:65148051-65148203 | Common:2; Rare:36 | ||||
chr1:65148887-65149091 | Common:4; Rare:61 | ||||
chr1:65254329-65254482 | Common:2; Rare:63 | ||||
chr1:65419916-65420118 | Rare:49 | ||||
chr1:65420191-65420725 | Common:6; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
chr1:66330374-66330774 | Common:5; Rare:65 | ||||
chr1:66331682-66331865 | Rare:35 | ||||
chr1:66331968-66332260 | Common:1; Rare:48 |