Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231241101-231241238 | Rare:72; Clinvar:2 | ||||
chr1:231528494-231528738 | Common:2; Rare:82 | ||||
chr1:232805318-232805425 | Common:2; Rare:61 | ||||
chr1:232950488-232950651 | Common:3; Rare:53 | ||||
chr1:234373351-234373578 | Common:1; Rare:113; Clinvar (benign):4 | ||||
chr1:234373636-234373775 | Rare:53; Clinvar (benign):3 | ||||
chr1:235328511-235328611 | Common:1; Rare:38 | ||||
chr1:235866910-235867116 | Common:2; Rare:51 | ||||
chr1:236604486-236604645 | Common:4; Rare:45 | ||||
chr1:236794996-236795312 | Common:5; Rare:107; Clinvar:1 | ||||
chr1:241519707-241519993 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:241848094-241848233 | Common:2; Rare:29 | ||||
chr1:243255047-243255142 | Rare:22 | ||||
chr1:243255176-243255422 | Common:1; Rare:53 | ||||
chr1:243255783-243256107 | Rare:86; Clinvar:4 |