Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:63367130-63367328 | Common:1; Rare:72 | ||||
chr18:63422352-63422646 | Common:1; Rare:78 | ||||
chr18:63970008-63970142 | Rare:28 | ||||
chr18:68714981-68715197 | Common:2; Rare:97 | ||||
chr18:70205659-70205790 | Common:3; Rare:53; Clinvar (benign):2 | ||||
chr18:74148352-74148614 | Common:1; Rare:76 | ||||
chr18:74496065-74496409 | Common:4; Rare:109 | ||||
chr18:79988331-79988645 | Common:3; Rare:109; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:572237-572629 | Common:3; Rare:193 | ||||
chr19:984232-984356 | Rare:44 | ||||
chr19:1103749-1104117 | Common:7; Rare:153 | ||||
chr19:1132191-1132314 | Rare:55 | ||||
chr19:2269238-2269601 | Common:2; Rare:153 | ||||
chr19:2328523-2328703 | Common:2; Rare:92 | ||||
chr19:2944917-2945175 | Common:5; Rare:90 |