Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70257902-70258167 | Common:1; Rare:83 | ||||
chr2:70293659-70293852 | Common:3; Rare:64 | ||||
chr2:71068534-71068672 | Rare:64 | ||||
chr2:71130225-71130588 | Common:5; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73071707-73071848 | Common:2; Rare:52 | ||||
chr2:73233200-73233539 | Common:1; Rare:98 | ||||
chr2:73737300-73737565 | Common:3; Rare:89 | ||||
chr2:73828804-73829036 | Common:1; Rare:54 | ||||
chr2:73926785-73926939 | Common:1; Rare:91; Clinvar:7; Clinvar (benign):3 | ||||
chr2:74147857-74148146 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178827-74179066 | Common:3; Rare:74 | ||||
chr2:74421591-74421781 | Rare:66 | ||||
chr2:74482916-74483093 | Common:1; Rare:56 | ||||
chr2:74529665-74530030 | Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74958529-74958701 | Common:4; Rare:63 |