Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:69387172-69387398 | Rare:60; Clinvar:2 | ||||
chr2:69643622-69643808 | Rare:65 | ||||
chr2:69829477-69829741 | Common:1; Rare:107 | ||||
chr2:69961594-69961789 | Rare:66 | ||||
chr2:70086931-70087118 | Common:1; Rare:93 | ||||
chr2:70087409-70087723 | Rare:119 | ||||
chr2:71068516-71068663 | Rare:76 | ||||
chr2:71129873-71130177 | Common:1; Rare:68 | ||||
chr2:71130224-71130662 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
chr2:72144373-72144678 | Common:3; Rare:65 | ||||
chr2:73071701-73071857 | Common:2; Rare:59 | ||||
chr2:73234140-73234368 | Common:2; Rare:65 | ||||
chr2:73385684-73386023 | Common:4; Rare:159; Clinvar:16; Clinvar (benign):8 | ||||
chr2:73828804-73829024 | Common:1; Rare:51 | ||||
chr2:74147870-74148115 | Common:1; Rare:64; Clinvar:2 |