Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:61017429-61017750 | Common:1; Rare:94; Clinvar:2 | ||||
chr2:61144926-61145164 | Common:3; Rare:79 | ||||
chr2:61888584-61888693 | Common:1; Rare:49 | ||||
chr2:63840822-63841154 | Common:2; Rare:91 | ||||
chr2:63841614-63841910 | Common:2; Rare:98 | ||||
chr2:65227579-65227852 | Rare:71 | ||||
chr2:68157496-68157890 | Common:2; Rare:197 | ||||
chr2:68467274-68467599 | Common:1; Rare:79 | ||||
chr2:69643641-69643877 | Rare:93 | ||||
chr2:70258014-70258158 | Common:1; Rare:48 | ||||
chr2:70293667-70293912 | Common:3; Rare:76 | ||||
chr2:71068539-71068654 | Rare:52 | ||||
chr2:71130227-71130322 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73071707-73071840 | Common:2; Rare:49 | ||||
chr2:73737297-73737493 | Common:2; Rare:61 |