Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:39437107-39437442 | Common:4; Rare:116 | ||||
chr2:43226598-43226853 | Common:1; Rare:99 | ||||
chr2:46616979-46617153 | Common:5; Rare:61 | ||||
chr2:61888590-61888700 | Common:1; Rare:46 | ||||
chr2:63840823-63841017 | Common:1; Rare:55 | ||||
chr2:65227603-65227852 | Rare:64 | ||||
chr2:70087373-70087762 | Common:2; Rare:152 | ||||
chr2:71130220-71130348 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74529632-74530036 | Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
chr2:74958876-74959071 | Rare:70 | ||||
chr2:85354550-85354772 | Common:1; Rare:67 | ||||
chr2:96265968-96266251 | Common:2; Rare:82; Clinvar:1 | ||||
chr2:98608447-98608629 | Common:1; Rare:79 | ||||
chr2:99181048-99181194 | Common:2; Rare:28 | ||||
chr2:113627079-113627269 | Common:1; Rare:53 |