Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27404046-27404330 | Common:3; Rare:42 | ||||
chr13:32175360-32175615 | Rare:57 | ||||
chr13:40664729-40664859 | Common:3; Rare:39 | ||||
chr13:40784574-40784892 | Rare:61 | ||||
chr13:44142001-44142361 | Common:6; Rare:60 | ||||
chr13:44404419-44404473 | Common:1; Rare:4 | ||||
chr13:45433704-45433720 | Rare:5 | ||||
chr13:45434681-45434849 | Common:1; Rare:21 | ||||
chr13:45447313-45447572 | Common:1; Rare:36 | ||||
chr13:46097213-46097239 | Rare:3 | ||||
chr13:46100329-46100469 | Rare:20 | ||||
chr13:46121230-46121372 | Rare:21 | ||||
chr13:48379875-48380082 | Common:4; Rare:35; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr13:50083031-50083138 | Rare:12 | ||||
chr13:50613402-50613612 | Common:1; Rare:38 |