Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149886501-149887223 | Common:3; Rare:275 | ||||
chr1:149887813-149888216 | Rare:130 | ||||
chr1:149917813-149917919 | Rare:31 | ||||
chr1:149927760-149927872 | Rare:49; Clinvar (benign):3 | ||||
chr1:150010685-150010837 | Common:1; Rare:36 | ||||
chr1:150067692-150067860 | Rare:54 | ||||
chr1:150150169-150150234 | Common:1; Rare:20 | ||||
chr1:150235933-150236368 | Common:1; Rare:97 | ||||
chr1:150257686-150257877 | Rare:46 | ||||
chr1:150321421-150321608 | Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364537-150364714 | Common:1; Rare:58 | ||||
chr1:150579171-150579272 | Rare:44 | ||||
chr1:150579595-150579892 | Common:10; Rare:93 | ||||
chr1:150629097-150629315 | Rare:64 | ||||
chr1:150629466-150629853 | Common:1; Rare:88 |