Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:146160977-146161315 | Common:2; Rare:109; Clinvar:5; Clinvar (benign):2 | ||||
chr3:148991455-148991620 | Common:2; Rare:75; Clinvar (benign):1 | ||||
chr3:149129545-149129688 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr3:149377570-149377869 | Common:1; Rare:69 | ||||
chr3:149657967-149658334 | Rare:86 | ||||
chr3:149812993-149813272 | Common:2; Rare:91 | ||||
chr3:150603204-150603422 | Common:2; Rare:95 | ||||
chr3:152268668-152268967 | Rare:120 | ||||
chr3:152269537-152269689 | Rare:40 | ||||
chr3:155870323-155870744 | Common:2; Rare:119 | ||||
chr3:156555019-156555406 | Common:2; Rare:148 | ||||
chr3:156674377-156674647 | Common:3; Rare:77 | ||||
chr3:157160123-157160285 | Rare:64 | ||||
chr3:157543242-157543391 | Rare:33 | ||||
chr3:158801815-158802146 | Common:3; Rare:115 |