Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147541231-147541583 | Common:2; Rare:57 | ||||
chr1:148458820-148459006 | Common:1; Rare:56 | ||||
chr1:148952264-148952654 | Common:5; Rare:106 | ||||
chr1:149812351-149812560 | Rare:66 | ||||
chr1:149850787-149851062 | Common:1; Rare:12 | ||||
chr1:149886632-149886959 | Common:1; Rare:119 | ||||
chr1:149887885-149888215 | Rare:101 | ||||
chr1:149917801-149917965 | Common:1; Rare:43 | ||||
chr1:149927764-149927922 | Common:1; Rare:62; Clinvar (benign):4 | ||||
chr1:150010692-150010966 | Common:1; Rare:75 | ||||
chr1:150067649-150067899 | Rare:71 | ||||
chr1:150257719-150257877 | Rare:34 | ||||
chr1:150293557-150293921 | Common:1; Rare:100 | ||||
chr1:150321393-150321592 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363964-150364239 | Common:3; Rare:95 |