Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:44119633-44119814 | Common:3; Rare:27 | ||||
chr3:45595486-45595776 | Common:3; Rare:93 | ||||
chr3:45953545-45953758 | Common:3; Rare:36 | ||||
chr3:45955335-45955474 | Rare:37; Clinvar (benign):1 | ||||
chr3:46111176-46111430 | Common:2; Rare:57 | ||||
chr3:46558352-46558636 | Common:3; Rare:52 | ||||
chr3:46672164-46672399 | Common:2; Rare:53 | ||||
chr3:47164794-47165068 | Common:2; Rare:58 | ||||
chr3:48088107-48088237 | Rare:25 | ||||
chr3:49101433-49101640 | Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr3:49356931-49357234 | Common:2; Rare:43 | ||||
chr3:50642229-50642276 | Rare:12 | ||||
chr3:52235187-52235370 | Common:1; Rare:28 | ||||
chr3:52407257-52407432 | Rare:47; Clinvar:3; Clinvar (benign):7 | ||||
chr3:52509696-52509979 | Common:1; Rare:72 |