Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:61017434-61017731 | Common:1; Rare:83; Clinvar:1 | ||||
chr2:61144926-61145160 | Common:2; Rare:76 | ||||
chr2:63588718-63588982 | Rare:81 | ||||
chr2:65227639-65227852 | Rare:56 | ||||
chr2:68157515-68157864 | Common:1; Rare:173 | ||||
chr2:69013295-69013424 | Rare:28 | ||||
chr2:69387190-69387404 | Rare:60; Clinvar:2 | ||||
chr2:71130225-71130298 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74198424-74198620 | Rare:72 | ||||
chr2:74529680-74529964 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
chr2:84459231-84459585 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4 | ||||
chr2:85354526-85354779 | Common:1; Rare:83 | ||||
chr2:85539047-85539168 | Common:1; Rare:47 | ||||
chr2:86106087-86106247 | Rare:48 | ||||
chr2:86195407-86195684 | Common:7; Rare:83 |