Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:38985701-38985890 | Common:1; Rare:18 | ||||
chr3:40453163-40453484 | Common:7; Rare:71 | ||||
chr3:42036543-42036682 | Rare:22 | ||||
chr3:42043053-42043257 | Rare:35 | ||||
chr3:46509356-46509575 | Rare:33 | ||||
chr3:49101831-49102062 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):6 | ||||
chr3:52046273-52046437 | Rare:26 | ||||
chr3:52046624-52046875 | Common:2; Rare:42 | ||||
chr3:52670758-52671027 | Rare:50 | ||||
chr3:54982699-54982819 | Rare:33 | ||||
chr3:55160229-55160410 | Common:1; Rare:26 | ||||
chr3:56692676-56692712 | Common:2; Rare:5 | ||||
chr3:56839865-56840023 | Common:1; Rare:32 | ||||
chr3:57013844-57013923 | Common:1; Rare:24 | ||||
chr3:57595918-57596026 | Rare:21 |