Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99606486-99606698 | Common:5; Rare:61 | ||||
chr13:100088894-100089135 | Rare:87; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674754-100675018 | Common:3; Rare:105 | ||||
chr13:102596794-102597059 | Common:1; Rare:123; Clinvar (benign):1 | ||||
chr13:102773736-102773860 | Rare:54 | ||||
chr13:102798991-102799124 | Rare:30 | ||||
chr13:102845614-102846089 | Common:9; Rare:127; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567769-106567926 | Rare:41 | ||||
chr13:106568072-106568258 | Rare:58 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110561664-110561911 | Common:5; Rare:88 | ||||
chr13:110615501-110615623 | Rare:45 | ||||
chr13:111153614-111153721 | Common:2; Rare:47 | ||||
chr13:112969146-112969233 | Common:2; Rare:27 | ||||
chr13:113208632-113208775 | Rare:81 |