Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26764193-26764357 | Common:2; Rare:64 | ||||
chr2:27032872-27033004 | Rare:51 | ||||
chr2:27211739-27212088 | Common:3; Rare:118 | ||||
chr2:27212210-27212398 | Common:2; Rare:101 | ||||
chr2:27282234-27282734 | Rare:90 | ||||
chr2:27282769-27282880 | Rare:27 | ||||
chr2:27323046-27323116 | Rare:16; Clinvar (benign):1 | ||||
chr2:27356750-27357199 | Common:2; Rare:136 | ||||
chr2:27370275-27370658 | Common:1; Rare:159 | ||||
chr2:27628954-27629113 | Common:1; Rare:89 | ||||
chr2:27663338-27663917 | Rare:179 | ||||
chr2:27771608-27772051 | Common:1; Rare:137 | ||||
chr2:27772223-27772383 | Rare:26 | ||||
chr2:27890354-27890839 | Common:1; Rare:134 | ||||
chr2:28392614-28392874 | Rare:86 |