Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32753842-32754034 | Common:2; Rare:69 | ||||
chr1:32817248-32817837 | Common:1; Rare:157; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818177-32818295 | Rare:35 | ||||
chr1:32901235-32901554 | Common:1; Rare:81 | ||||
chr1:33021372-33021704 | Rare:81; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:33036802-33037104 | Rare:114; Clinvar (pathogenic):2 | ||||
chr1:33080992-33081203 | Common:2; Rare:63 | ||||
chr1:33182057-33182373 | Rare:66 | ||||
chr1:34985286-34985380 | Common:1; Rare:34 | ||||
chr1:35031638-35031771 | Common:1; Rare:41 | ||||
chr1:35079317-35079422 | Common:3; Rare:30 | ||||
chr1:35192467-35192742 | Common:3; Rare:92 | ||||
chr1:35192978-35193239 | Common:1; Rare:100 | ||||
chr1:35268514-35269061 | Rare:186 | ||||
chr1:35557345-35557481 | Common:1; Rare:40 |