Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151346692-151347092 | Rare:435 | ||||
chr1:151347172-151347606 | Rare:398 | ||||
chr1:151370200-151371040 | Common:11; Rare:292 | ||||
chr1:151372270-151372935 | Common:7; Rare:232 | ||||
chr1:151399330-151399800 | Common:14; Rare:429; Clinvar (pathogenic):7 | ||||
chr1:151458083-151459204 | Common:33; Rare:1071 | ||||
chr1:151459370-151459770 | Common:2; Rare:256 | ||||
chr1:151511130-151511490 | Common:4; Rare:83 | ||||
chr1:151539590-151539950 | Rare:112 | ||||
chr1:151540047-151540447 | Common:3; Rare:260 | ||||
chr1:151611563-151612343 | Common:19; Rare:450; Clinvar:3; Clinvar (benign):4 | ||||
chr1:151762145-151763150 | Common:15; Rare:522 | ||||
chr1:151763170-151763900 | Common:18; Rare:597 | ||||
chr1:151763949-151764611 | Common:4; Rare:118 | ||||
chr1:151789966-151790366 | Common:3; Rare:85 |