Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70190980-70191119 | Rare:32 | ||||
chr2:70248552-70248814 | Common:5; Rare:98 | ||||
chr2:70257977-70258242 | Common:2; Rare:93 | ||||
chr2:70293661-70293838 | Common:2; Rare:60 | ||||
chr2:71068543-71068679 | Rare:57 | ||||
chr2:71130224-71130677 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73234220-73234361 | Common:1; Rare:44 | ||||
chr2:73385581-73385860 | Common:2; Rare:105; Clinvar:6; Clinvar (benign):3 | ||||
chr2:73737300-73737507 | Common:3; Rare:67 | ||||
chr2:73828889-73829037 | Rare:39 | ||||
chr2:74147870-74148091 | Common:1; Rare:59; Clinvar:2 | ||||
chr2:74178796-74179009 | Common:2; Rare:58 | ||||
chr2:74421579-74421768 | Rare:65 | ||||
chr2:74440413-74440642 | Rare:60 | ||||
chr2:74441859-74442053 | Common:2; Rare:41 |