Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32753867-32754020 | Common:1; Rare:51 | ||||
chr1:32817266-32817800 | Common:1; Rare:146; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32895303-32895915 | Common:2; Rare:196 | ||||
chr1:33080994-33081174 | Common:1; Rare:45 | ||||
chr1:34985245-34985393 | Common:1; Rare:57 | ||||
chr1:35031667-35031996 | Common:1; Rare:97 | ||||
chr1:35192413-35192723 | Common:2; Rare:92 | ||||
chr1:35557353-35557442 | Rare:25 | ||||
chr1:35557629-35557863 | Common:2; Rare:93 | ||||
chr1:35930505-35930774 | Common:1; Rare:70 | ||||
chr1:36149420-36149800 | Common:2; Rare:107 | ||||
chr1:36155887-36156180 | Rare:112 | ||||
chr1:36171303-36171574 | Common:1; Rare:66 | ||||
chr1:36177900-36178586 | Common:5; Rare:205 | ||||
chr1:36224097-36224499 | Common:1; Rare:124 |