Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62688069-62688569 | Common:2; Rare:178; Clinvar:1 | ||||
chr1:62783735-62783911 | Rare:35 | ||||
chr1:62784018-62784258 | Rare:84 | ||||
chr1:62784519-62784590 | Rare:14 | ||||
chr1:63367265-63367760 | Common:1; Rare:134; Clinvar (benign):1 | ||||
chr1:63367874-63368072 | Common:2; Rare:35 | ||||
chr1:63523174-63523684 | Common:4; Rare:131 | ||||
chr1:63523821-63523871 | Rare:8 | ||||
chr1:63523969-63524019 | Rare:12 | ||||
chr1:63547669-63548033 | Common:3; Rare:56 | ||||
chr1:63593115-63593463 | Rare:113; Clinvar (benign):1 | ||||
chr1:63593562-63594156 | Common:6; Rare:211; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:63594157-63594652 | Common:7; Rare:113 | ||||
chr1:63773869-63774292 | Rare:83 | ||||
chr1:63774842-63774966 | Common:1; Rare:27 |