Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26244601-26244943 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):6 | ||||
chr2:26345798-26346156 | Common:1; Rare:107 | ||||
chr2:27032852-27032995 | Rare:56 | ||||
chr2:27071549-27071864 | Common:1; Rare:92 | ||||
chr2:27078522-27078683 | Common:2; Rare:44 | ||||
chr2:27211771-27212103 | Common:3; Rare:115 | ||||
chr2:27212229-27212366 | Common:1; Rare:74 | ||||
chr2:27323050-27323121 | Rare:15; Clinvar (benign):1 | ||||
chr2:27356750-27356800 | Rare:10 | ||||
chr2:27356970-27357077 | Rare:42 | ||||
chr2:27370275-27370641 | Common:1; Rare:151 | ||||
chr2:27583010-27583101 | Rare:35 | ||||
chr2:27628848-27629098 | Common:1; Rare:106 | ||||
chr2:27663395-27663424 | Rare:7 | ||||
chr2:27663592-27663911 | Rare:113 |