Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26033785-26034142 | Common:3; Rare:124 | ||||
chr2:26244561-26244975 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26345798-26346156 | Common:1; Rare:107 | ||||
chr2:27032867-27033009 | Rare:53 | ||||
chr2:27071604-27071953 | Common:2; Rare:99 | ||||
chr2:27212261-27212393 | Common:2; Rare:70 | ||||
chr2:27323058-27323121 | Rare:13 | ||||
chr2:27356746-27356856 | Rare:27 | ||||
chr2:27356979-27357087 | Rare:40 | ||||
chr2:27370310-27370633 | Common:1; Rare:127 | ||||
chr2:27582970-27583112 | Rare:54 | ||||
chr2:27628981-27629077 | Common:1; Rare:49 | ||||
chr2:27663395-27663469 | Rare:17 | ||||
chr2:27663537-27663911 | Rare:132 | ||||
chr2:27890443-27890802 | Rare:89 |