Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49491486-49491785 | Common:1; Rare:95 | ||||
chr19:49635754-49635972 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
chr19:52923405-52923542 | Common:3; Rare:57 | ||||
chr19:52942563-52942782 | Common:7; Rare:78 | ||||
chr2:1679871-1679939 | Rare:16 | ||||
chr2:3536486-3536626 | Common:2; Rare:25 | ||||
chr2:13000838-13000936 | Rare:25 | ||||
chr2:13006982-13007233 | Common:4; Rare:47 | ||||
chr2:19353663-19353993 | Common:1; Rare:87 | ||||
chr2:20447729-20447955 | Rare:68 | ||||
chr2:20448113-20448233 | Rare:33 | ||||
chr2:20448362-20448827 | Common:2; Rare:115 | ||||
chr2:28301047-28301353 | Common:1; Rare:48 | ||||
chr2:28391704-28391817 | Rare:26 | ||||
chr2:36544166-36544496 | Common:2; Rare:94 |