Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72781853-72782191 | Common:1; Rare:131 | ||||
chr13:76886402-76886661 | Common:2; Rare:82 | ||||
chr13:100088935-100089127 | Rare:72; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674772-100675056 | Common:3; Rare:116 | ||||
chr13:102596785-102597028 | Common:1; Rare:113 | ||||
chr13:102798918-102799144 | Common:1; Rare:49 | ||||
chr13:106568094-106568267 | Rare:56 | ||||
chr13:108218304-108218499 | Rare:71 | ||||
chr13:110307107-110307496 | Common:6; Rare:125; Clinvar (benign):8 | ||||
chr13:112588122-112588354 | Rare:55 | ||||
chr13:113208625-113208741 | Rare:68 | ||||
chr13:113490739-113491158 | Common:4; Rare:159 | ||||
chr13:113863959-113864180 | Common:2; Rare:59 | ||||
chr14:20454804-20455323 | Common:7; Rare:135 | ||||
chr14:20455457-20455690 | Rare:69 |