Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26695646-26695762 | Rare:41 | ||||
chr1:26695886-26696099 | Rare:65 | ||||
chr1:26771670-26771990 | Common:1; Rare:67 | ||||
chr1:26786932-26787117 | Rare:43 | ||||
chr1:26787837-26788322 | Common:3; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26826572-26826786 | Rare:73 | ||||
chr1:26862827-26863235 | Rare:91 | ||||
chr1:26863497-26864070 | Common:4; Rare:254 | ||||
chr1:26889586-26889986 | Rare:207 | ||||
chr1:26890210-26890392 | Common:1; Rare:76 | ||||
chr1:26900052-26900220 | Rare:63 | ||||
chr1:26900399-26900571 | Rare:63 | ||||
chr1:26921505-26921825 | Common:3; Rare:95 | ||||
chr1:26960377-26960570 | Common:1; Rare:44 | ||||
chr1:26993523-26993739 | Common:5; Rare:75 |