Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650908-32651369 | Common:2; Rare:172 | ||||
chr1:32651444-32651663 | Common:6; Rare:64 | ||||
chr1:32817180-32817753 | Common:1; Rare:154; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818000-32818483 | Common:1; Rare:126 | ||||
chr1:32963953-32964254 | Rare:63 | ||||
chr1:32964793-32965075 | Common:2; Rare:102 | ||||
chr1:33036785-33037122 | Rare:127; Clinvar (pathogenic):2 | ||||
chr1:33080911-33081169 | Common:2; Rare:61 | ||||
chr1:33181997-33182085 | Rare:16 | ||||
chr1:33256227-33256502 | Common:1; Rare:70 | ||||
chr1:33349207-33349251 | Rare:6 | ||||
chr1:33349829-33350161 | Common:2; Rare:112 | ||||
chr1:33472349-33472597 | Common:1; Rare:51 | ||||
chr1:34859661-34859947 | Common:1; Rare:72 | ||||
chr1:34984678-34985037 | Common:3; Rare:83 |