Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20446841-20447074 | Common:3; Rare:93 | ||||
chr2:20651061-20651271 | Rare:66 | ||||
chr2:23927073-23927301 | Common:3; Rare:83 | ||||
chr2:23940379-23940539 | Common:3; Rare:60 | ||||
chr2:24076244-24076594 | Rare:95 | ||||
chr2:24123313-24123478 | Common:1; Rare:42 | ||||
chr2:25878453-25878737 | Common:3; Rare:87 | ||||
chr2:26033748-26034159 | Common:4; Rare:155 | ||||
chr2:26244593-26244984 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345831-26346187 | Common:1; Rare:103 | ||||
chr2:26764218-26764325 | Rare:41 | ||||
chr2:27032872-27032983 | Rare:40 | ||||
chr2:27071516-27071878 | Common:1; Rare:109 | ||||
chr2:27211747-27212095 | Common:3; Rare:118 | ||||
chr2:27212252-27212364 | Common:1; Rare:57 |