Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:157160134-157160327 | Rare:80 | ||||
chr3:158105761-158105872 | Common:5; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158801923-158802146 | Common:3; Rare:95 | ||||
chr3:160399518-160399692 | Rare:40 | ||||
chr3:160565564-160565784 | Common:2; Rare:77 | ||||
chr3:167734849-167735181 | Common:2; Rare:104 | ||||
chr3:169773336-169773405 | Rare:17 | ||||
chr3:170908590-170908842 | Common:1; Rare:71 | ||||
chr3:172040384-172040579 | Common:1; Rare:49 | ||||
chr3:179347600-179347761 | Common:1; Rare:37 | ||||
chr3:179604632-179604836 | Common:1; Rare:65 | ||||
chr3:182793334-182793638 | Common:3; Rare:82 | ||||
chr3:184135221-184135385 | Common:2; Rare:48; Clinvar:5 | ||||
chr3:184249527-184249682 | Rare:42 | ||||
chr3:184298979-184299283 | Common:2; Rare:91 |