Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74465324-74465439 | Rare:32; Clinvar:1 | ||||
chr2:74482958-74483093 | Common:1; Rare:45 | ||||
chr2:74529676-74529942 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74553905-74554163 | Rare:54 | ||||
chr2:74833825-74834147 | Common:1; Rare:96 | ||||
chr2:74958695-74959091 | Common:1; Rare:155 | ||||
chr2:75710675-75710782 | Common:1; Rare:43 | ||||
chr2:75710887-75711020 | Rare:46 | ||||
chr2:84459170-84459338 | Rare:69; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:85327951-85328056 | Common:1; Rare:51 | ||||
chr2:85354522-85354812 | Common:1; Rare:96 | ||||
chr2:85539019-85539368 | Common:3; Rare:169; Clinvar (benign):7 | ||||
chr2:85561428-85561561 | Rare:49; Clinvar:4 | ||||
chr2:85595565-85595779 | Common:1; Rare:71 | ||||
chr2:85602662-85602915 | Rare:60 |