Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73828792-73829029 | Common:1; Rare:55 | ||||
chr2:74002570-74002698 | Common:2; Rare:51 | ||||
chr2:74147866-74148143 | Common:1; Rare:70; Clinvar:2 | ||||
chr2:74178779-74179009 | Common:2; Rare:60 | ||||
chr2:74421579-74421768 | Rare:65 | ||||
chr2:74441875-74442108 | Common:2; Rare:41 | ||||
chr2:74458113-74458486 | Common:1; Rare:114 | ||||
chr2:74465354-74465459 | Common:1; Rare:27 | ||||
chr2:74482904-74483095 | Common:1; Rare:61 | ||||
chr2:74507664-74507790 | Rare:27 | ||||
chr2:74529614-74530025 | Rare:135; Clinvar:4; Clinvar (benign):1 | ||||
chr2:74554636-74554755 | Common:1; Rare:48 | ||||
chr2:74958509-74958682 | Common:3; Rare:63 | ||||
chr2:74958872-74959071 | Rare:72 | ||||
chr2:75199518-75199613 | Rare:14 |