Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149917801-149917971 | Common:1; Rare:44 | ||||
chr1:149927734-149927895 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:150010697-150010933 | Common:1; Rare:67 | ||||
chr1:150067656-150067852 | Rare:57 | ||||
chr1:150268816-150268835 | Common:2; Rare:8 | ||||
chr1:150272382-150272752 | Common:1; Rare:63 | ||||
chr1:150282309-150282596 | Common:3; Rare:56 | ||||
chr1:150293822-150293913 | Rare:30 | ||||
chr1:150321424-150321592 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364610-150364717 | Rare:37 | ||||
chr1:150487279-150487444 | Common:3; Rare:37; Clinvar (benign):3 | ||||
chr1:150578473-150578779 | Common:1; Rare:90 | ||||
chr1:150579595-150579897 | Common:10; Rare:93 | ||||
chr1:150629522-150629827 | Rare:60 | ||||
chr1:150876554-150876832 | Common:5; Rare:108 |