Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102845741-102846084 | Common:8; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567575-106567673 | Rare:34 | ||||
chr13:106568094-106568273 | Rare:56 | ||||
chr13:108215370-108215633 | Common:5; Rare:50 | ||||
chr13:108218307-108218525 | Rare:82 | ||||
chr13:110307110-110307496 | Common:6; Rare:124; Clinvar (benign):8 | ||||
chr13:110307590-110308118 | Common:4; Rare:172 | ||||
chr13:110615385-110615656 | Common:2; Rare:93 | ||||
chr13:110713487-110713679 | Common:2; Rare:81 | ||||
chr13:112588135-112588283 | Rare:35 | ||||
chr13:113208169-113208304 | Common:2; Rare:31 | ||||
chr13:113208594-113208769 | Rare:104 | ||||
chr13:113297047-113297321 | Common:1; Rare:105 | ||||
chr13:113490661-113491258 | Common:5; Rare:217 | ||||
chr13:113759150-113759255 | Rare:29 |