Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:22817353-22817469 | Rare:31 | ||||
chr2:25517739-25518123 | Common:3; Rare:59 | ||||
chr2:25529132-25529369 | Common:1; Rare:36 | ||||
chr2:26191481-26191848 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:26757938-26758269 | Rare:57 | ||||
chr2:28611208-28611447 | Common:1; Rare:53 | ||||
chr2:28783789-28783943 | Rare:34 | ||||
chr2:29106392-29106540 | Common:2; Rare:22 | ||||
chr2:29129940-29130110 | Common:2; Rare:40 | ||||
chr2:29455176-29455300 | Rare:22 | ||||
chr2:29455388-29455851 | Common:1; Rare:78 | ||||
chr2:29718331-29718583 | Rare:48 | ||||
chr2:30135658-30135797 | Rare:22 | ||||
chr2:32275728-32276016 | Common:1; Rare:73 | ||||
chr2:33706670-33706931 | Common:2; Rare:55 |