Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151299064-151299182 | Common:2; Rare:21 | ||||
chr1:151327350-151327460 | Common:2; Rare:35 | ||||
chr1:151327603-151327818 | Common:2; Rare:41 | ||||
chr1:151346839-151347029 | Rare:54 | ||||
chr1:151347170-151347340 | Rare:38 | ||||
chr1:151399480-151399635 | Common:2; Rare:59; Clinvar (pathogenic):2 | ||||
chr1:151459143-151459538 | Common:3; Rare:146 | ||||
chr1:151511092-151511417 | Common:4; Rare:75 | ||||
chr1:151611900-151612280 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
chr1:151761492-151761763 | Common:2; Rare:66 | ||||
chr1:151763433-151763522 | Common:2; Rare:33 | ||||
chr1:151790422-151790871 | Common:3; Rare:109 | ||||
chr1:151831739-151831859 | Rare:29 | ||||
chr1:151909397-151909709 | Common:4; Rare:111 | ||||
chr1:152325234-152325445 | Common:1; Rare:36 |