Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151327295-151327470 | Common:2; Rare:49 | ||||
chr1:151327615-151327885 | Common:3; Rare:52 | ||||
chr1:151346268-151346337 | Rare:20; Clinvar:1 | ||||
chr1:151346751-151346771 | Rare:2 | ||||
chr1:151346774-151347669 | Rare:200 | ||||
chr1:151399225-151399634 | Common:9; Rare:106; Clinvar (pathogenic):2 | ||||
chr1:151458481-151458934 | Common:5; Rare:229 | ||||
chr1:151459082-151459211 | Common:1; Rare:38 | ||||
chr1:151459423-151459571 | Rare:59 | ||||
chr1:151511111-151511403 | Common:3; Rare:67 | ||||
chr1:151540133-151540354 | Common:1; Rare:72 | ||||
chr1:151611876-151612247 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr1:151720740-151721063 | Rare:45 | ||||
chr1:151721465-151721522 | Rare:16 | ||||
chr1:151763027-151763144 | Common:2; Rare:45 |