Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:139109299-139109393 | Rare:30 | ||||
chr7:139109712-139109821 | Common:1; Rare:28 | ||||
chr7:139359660-139359982 | Common:3; Rare:133 | ||||
chr7:141738021-141738619 | Common:5; Rare:167 | ||||
chr7:143288051-143288353 | Common:1; Rare:88 | ||||
chr7:143380853-143381102 | Common:1; Rare:67 | ||||
chr7:143382631-143382926 | Common:1; Rare:106 | ||||
chr7:144835979-144836140 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr7:148698426-148698980 | Common:5; Rare:187 | ||||
chr7:149028622-149028974 | Common:2; Rare:119 | ||||
chr7:149090682-149090876 | Rare:51 | ||||
chr7:149126229-149126438 | Common:6; Rare:71 | ||||
chr7:149873852-149874058 | Common:3; Rare:80 | ||||
chr7:150379084-150379365 | Common:1; Rare:94 | ||||
chr7:150632263-150632513 | Common:3; Rare:46 |