Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:17161221-17161288 | Common:1; Rare:19 | ||||
chr3:17167813-17167964 | Rare:33 | ||||
chr3:28136958-28137142 | Common:1; Rare:22 | ||||
chr3:29642807-29643029 | Rare:31 | ||||
chr3:38252734-38252934 | Rare:55 | ||||
chr3:38455347-38455539 | Common:1; Rare:44 | ||||
chr3:38459257-38459448 | Rare:41 | ||||
chr3:39384289-39384431 | Common:3; Rare:24 | ||||
chr3:40453163-40453435 | Common:6; Rare:61 | ||||
chr3:41225468-41225727 | Rare:53; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:42654383-42654609 | Rare:69 | ||||
chr3:44357533-44357813 | Rare:60 | ||||
chr3:45211879-45212056 | Rare:40 | ||||
chr3:46948256-46948449 | Common:5; Rare:42 | ||||
chr3:47407260-47407573 | Common:2; Rare:86 |