Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26033776-26034195 | Common:4; Rare:153 | ||||
chr2:26244581-26244975 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):9 | ||||
chr2:26345819-26346156 | Common:1; Rare:100 | ||||
chr2:26764210-26764325 | Rare:44 | ||||
chr2:27032862-27033004 | Rare:55 | ||||
chr2:27211739-27212065 | Common:3; Rare:113 | ||||
chr2:27212257-27212386 | Common:2; Rare:65 | ||||
chr2:27323051-27323115 | Rare:15; Clinvar (benign):1 | ||||
chr2:27356754-27356854 | Rare:25 | ||||
chr2:27356976-27357170 | Common:2; Rare:67 | ||||
chr2:27370310-27370636 | Common:1; Rare:129 | ||||
chr2:27582982-27583101 | Rare:44 | ||||
chr2:27628981-27629073 | Common:1; Rare:45 | ||||
chr2:27663395-27663451 | Rare:13 | ||||
chr2:27663545-27663911 | Rare:131 |