Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168179144-168179371 | Rare:55 | ||||
chr1:168179376-168179487 | Rare:28 | ||||
chr1:168225281-168225536 | Common:3; Rare:51 | ||||
chr1:168225700-168226123 | Common:4; Rare:138 | ||||
chr1:169105650-169105856 | Common:1; Rare:49 | ||||
chr1:169106174-169106456 | Common:3; Rare:108 | ||||
chr1:169106534-169106794 | Common:1; Rare:100 | ||||
chr1:169107616-169107971 | Common:3; Rare:80 | ||||
chr1:169309689-169309774 | Rare:17 | ||||
chr1:169367689-169368013 | Common:2; Rare:81 | ||||
chr1:169368152-169368306 | Common:1; Rare:35 | ||||
chr1:169427472-169427509 | Rare:6 | ||||
chr1:169485669-169486242 | Common:2; Rare:165; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169711495-169711686 | Rare:64 | ||||
chr1:169794634-169794797 | Common:2; Rare:33 |