Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42766506-42766722 | Rare:55; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42766970-42767311 | Common:4; Rare:114; Clinvar (benign):1 | ||||
chr1:42816961-42817139 | Common:1; Rare:52 | ||||
chr1:42817185-42817631 | Rare:132 | ||||
chr1:42846384-42846650 | Common:1; Rare:77 | ||||
chr1:42958771-42959097 | Common:4; Rare:86; Clinvar:6; Clinvar (benign):4 | ||||
chr1:42959160-42959532 | Common:2; Rare:81 | ||||
chr1:43172214-43172375 | Common:1; Rare:75 | ||||
chr1:43300700-43301286 | Common:4; Rare:105 | ||||
chr1:43302008-43302541 | Common:3; Rare:95 | ||||
chr1:43302682-43302878 | Rare:33 | ||||
chr1:43306897-43307572 | Common:1; Rare:206 | ||||
chr1:43307791-43308622 | Common:4; Rare:142 | ||||
chr1:43308650-43308699 | Common:1; Rare:11 | ||||
chr1:43308986-43309533 | Common:2; Rare:152 |