Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36999254-36999451 | Rare:81 | ||||
chr13:37000250-37000422 | Common:2; Rare:32 | ||||
chr13:37000698-37000815 | Rare:48; Clinvar (pathogenic):1 | ||||
chr13:37059590-37059782 | Common:1; Rare:66 | ||||
chr13:37869765-37869926 | Common:1; Rare:37 | ||||
chr13:39038079-39038439 | Common:1; Rare:88 | ||||
chr13:39655583-39655802 | Common:4; Rare:110; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr13:40771138-40771346 | Common:3; Rare:68 | ||||
chr13:40789368-40789635 | Common:2; Rare:89; Clinvar:6; Clinvar (benign):2 | ||||
chr13:41060846-41061645 | Common:20; Rare:326 | ||||
chr13:41132732-41132949 | Rare:57 | ||||
chr13:41311197-41311306 | Rare:47 | ||||
chr13:41457254-41457547 | Common:2; Rare:79 | ||||
chr13:42271944-42272170 | Common:1; Rare:51 | ||||
chr13:43023443-43023724 | Common:1; Rare:99 |