Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:33285710-33285887 | Rare:41 | ||||
chr13:33817992-33818226 | Common:1; Rare:107 | ||||
chr13:36345543-36345657 | Common:1; Rare:23 | ||||
chr13:36346260-36346454 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36346627-36347038 | Common:4; Rare:107 | ||||
chr13:36999272-36999448 | Rare:70 | ||||
chr13:37000575-37000815 | Common:1; Rare:81; Clinvar (pathogenic):1 | ||||
chr13:37059583-37059726 | Common:1; Rare:49 | ||||
chr13:38350214-38350287 | Rare:37 | ||||
chr13:39038064-39038433 | Common:1; Rare:92 | ||||
chr13:39655642-39655750 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr13:40789377-40789628 | Common:2; Rare:84; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41061352-41061645 | Common:2; Rare:91 | ||||
chr13:41132732-41132997 | Rare:72 | ||||
chr13:42271722-42272198 | Common:4; Rare:125 |