Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11262440-11262980 | Common:16; Rare:740 | ||||
chr1:11272853-11273309 | Common:2; Rare:319; Clinvar:3; Clinvar (benign):3 | ||||
chr1:11273496-11274373 | Common:2; Rare:647; Clinvar:7; Clinvar (benign):13; Clinvar (pathogenic):15 | ||||
chr1:11650350-11650890 | Common:4; Rare:213 | ||||
chr1:11654164-11654564 | Common:1; Rare:168 | ||||
chr1:11654600-11655260 | Common:20; Rare:381 | ||||
chr1:11663810-11664420 | Common:4; Rare:259 | ||||
chr1:11680397-11681830 | Common:49; Rare:1691 | ||||
chr1:11735853-11736790 | Common:23; Rare:858 | ||||
chr1:11761930-11762340 | Common:4; Rare:303 | ||||
chr1:11785083-11785557 | Common:13; Rare:256 | ||||
chr1:11787519-11787934 | Common:16; Rare:279; Clinvar:16; Clinvar (benign):12 | ||||
chr1:11802662-11802830 | Common:5; Rare:117 | ||||
chr1:11803080-11803320 | Common:2; Rare:113; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr1:11803408-11803890 | Common:5; Rare:329 |