Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150364590-150364717 | Rare:46 | ||||
chr1:150579208-150579271 | Rare:28 | ||||
chr1:150629528-150629857 | Common:1; Rare:71 | ||||
chr1:150926249-150926339 | Rare:21 | ||||
chr1:151165840-151166166 | Common:3; Rare:90 | ||||
chr1:151254612-151254791 | Rare:43 | ||||
chr1:151399452-151399608 | Common:2; Rare:53; Clinvar (pathogenic):1 | ||||
chr1:151763451-151763541 | Common:1; Rare:33 | ||||
chr1:153535955-153536157 | Common:1; Rare:47 | ||||
chr1:153608937-153609055 | Common:1; Rare:21 | ||||
chr1:153670926-153671209 | Rare:87 | ||||
chr1:153958577-153958846 | Common:1; Rare:82 | ||||
chr1:153963500-153963738 | Common:1; Rare:64 | ||||
chr1:153986223-153986416 | Rare:50 | ||||
chr1:153990660-153990826 | Common:2; Rare:81 |