Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148428422-148428673 | Common:1; Rare:61 | ||||
chr1:148459807-148459852 | Rare:10 | ||||
chr1:148522297-148522611 | Common:4; Rare:80 | ||||
chr1:148952963-148953246 | Common:3; Rare:130 | ||||
chr1:148953552-148953849 | Common:1; Rare:118 | ||||
chr1:149176004-149176102 | Common:1; Rare:18 | ||||
chr1:149176345-149176636 | Common:4; Rare:43 | ||||
chr1:149176844-149176935 | Common:1; Rare:30 | ||||
chr1:149636392-149636760 | Common:10; Rare:112 | ||||
chr1:150555864-150556174 | Rare:73; Clinvar:1 | ||||
chr1:150556737-150557045 | Common:1; Rare:98; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:150559033-150559377 | Common:1; Rare:123; Clinvar:3 | ||||
chr1:150561310-150561650 | Common:1; Rare:90 | ||||
chr1:150561687-150561780 | Rare:19 | ||||
chr1:150620032-150620190 | Rare:30 |