Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:45995785-45995961 | Common:2; Rare:39; Clinvar:1 | ||||
chr3:46693665-46693817 | Common:1; Rare:34 | ||||
chr3:46882156-46882505 | Common:1; Rare:103 | ||||
chr3:46979569-46979820 | Common:1; Rare:56; Clinvar:1 | ||||
chr3:47163933-47164213 | Common:1; Rare:75 | ||||
chr3:47380803-47381083 | Rare:93 | ||||
chr3:47475812-47476051 | Common:3; Rare:103 | ||||
chr3:47513669-47513767 | Rare:33 | ||||
chr3:47781682-47782003 | Rare:115 | ||||
chr3:47802896-47803199 | Common:1; Rare:87 | ||||
chr3:48440067-48440312 | Common:1; Rare:95 | ||||
chr3:48918783-48918920 | Common:2; Rare:80 | ||||
chr3:49021498-49021710 | Rare:52; Clinvar:1 | ||||
chr3:49029381-49029564 | Common:2; Rare:128 | ||||
chr3:49104738-49104910 | Rare:69; Clinvar (benign):3 |