Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:5691209-5691455 | Rare:64 | ||||
chr2:5691696-5692032 | Common:7; Rare:96 | ||||
chr2:5693546-5694295 | Common:1; Rare:194; Clinvar:1; Clinvar (benign):1 | ||||
chr2:5694298-5694547 | Common:3; Rare:42 | ||||
chr2:5694746-5695102 | Common:3; Rare:39 | ||||
chr2:5695840-5696094 | Common:1; Rare:53 | ||||
chr2:5696766-5697155 | Common:4; Rare:143 | ||||
chr2:5700891-5701029 | Rare:36 | ||||
chr2:5726042-5726171 | Rare:25 | ||||
chr2:5981594-5981802 | Rare:32 | ||||
chr2:5981844-5981999 | Rare:32 | ||||
chr2:5982346-5982673 | Common:1; Rare:68 | ||||
chr2:6053707-6053948 | Rare:39 | ||||
chr2:6079311-6079532 | Common:2; Rare:34 | ||||
chr2:6918646-6918695 | Common:1; Rare:8 |