Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153977598-153977835 | Rare:65 | ||||
chr1:153977998-153978028 | Rare:5 | ||||
chr1:153985386-153985567 | Rare:27 | ||||
chr1:153986123-153986320 | Rare:52 | ||||
chr1:153986321-153986485 | Common:1; Rare:41 | ||||
chr1:153986855-153987024 | Common:2; Rare:29 | ||||
chr1:153990618-153990825 | Common:2; Rare:91 | ||||
chr1:154182238-154182813 | Common:1; Rare:124 | ||||
chr1:154183140-154183410 | Rare:87 | ||||
chr1:154220489-154221043 | Common:1; Rare:183 | ||||
chr1:154221409-154221616 | Rare:51 | ||||
chr1:154272248-154272692 | Common:6; Rare:96; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154405057-154405253 | Common:3; Rare:30 | ||||
chr1:154405378-154405425 | Common:1; Rare:5 | ||||
chr1:154405457-154405804 | Rare:79 |