Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:68467292-68467594 | Common:1; Rare:72 | ||||
chr2:69387123-69387398 | Rare:76; Clinvar:2 | ||||
chr2:69437395-69437654 | Common:1; Rare:129; Clinvar:6; Clinvar (benign):3 | ||||
chr2:69643622-69643883 | Rare:97 | ||||
chr2:69829541-69829676 | Rare:52 | ||||
chr2:70087400-70087750 | Common:1; Rare:135 | ||||
chr2:70293665-70293806 | Common:2; Rare:45 | ||||
chr2:71068539-71068672 | Rare:59 | ||||
chr2:71130225-71130659 | Common:6; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71453485-71453708 | Common:1; Rare:45 | ||||
chr2:71453856-71453912 | Rare:11 | ||||
chr2:72144469-72144710 | Common:3; Rare:55 | ||||
chr2:73234168-73234356 | Common:2; Rare:53 | ||||
chr2:73737276-73737461 | Common:2; Rare:54 | ||||
chr2:73828818-73829029 | Common:1; Rare:49 |