Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38009165-38009348 | Rare:33 | ||||
chr1:38012537-38012831 | Rare:90 | ||||
chr1:38873297-38873566 | Common:3; Rare:95 | ||||
chr1:39026231-39026398 | Common:1; Rare:45 | ||||
chr1:39215056-39215285 | Rare:40 | ||||
chr1:39738739-39738919 | Common:2; Rare:44 | ||||
chr1:39883454-39883570 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
chr1:40039875-40040119 | Common:2; Rare:56 | ||||
chr1:40040444-40040806 | Common:3; Rare:110 | ||||
chr1:40097234-40097319 | Rare:33; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40161265-40161409 | Rare:38 | ||||
chr1:40257898-40258282 | Common:4; Rare:105; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40373542-40373811 | Common:1; Rare:67 | ||||
chr1:40449922-40450174 | Common:4; Rare:97 | ||||
chr1:40508626-40508794 | Common:5; Rare:51 |