Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:95676894-95677280 | Common:4; Rare:144 | ||||
chr13:96053325-96053512 | Common:2; Rare:85 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:100088901-100089135 | Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596773-102597051 | Common:1; Rare:129; Clinvar (benign):1 | ||||
chr13:102798945-102799130 | Common:1; Rare:40 | ||||
chr13:102845719-102846084 | Common:9; Rare:98; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106568072-106568215 | Rare:49 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110307154-110307526 | Common:5; Rare:108; Clinvar (benign):6 | ||||
chr13:110561641-110561889 | Common:5; Rare:84 | ||||
chr13:110615432-110615661 | Rare:79 | ||||
chr13:110713008-110713266 | Common:2; Rare:114 | ||||
chr13:111153569-111153713 | Common:2; Rare:65 | ||||
chr13:112968173-112968476 | Rare:64 |