Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:48381267-48381294 | Rare:9 | ||||
chr16:54270813-54271004 | Rare:32 | ||||
chr16:56683552-56683884 | Common:7; Rare:56 | ||||
chr16:57266928-57267119 | Common:2; Rare:36 | ||||
chr16:57630444-57630564 | Common:2; Rare:36 | ||||
chr16:57651283-57651859 | Rare:170; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
chr16:57789255-57789351 | Rare:20 | ||||
chr16:58450133-58450216 | Rare:15 | ||||
chr16:58528580-58528791 | Rare:32 | ||||
chr16:67429552-67429817 | Common:1; Rare:41 | ||||
chr16:67432144-67432390 | Rare:62 | ||||
chr16:67434040-67434299 | Common:1; Rare:35 | ||||
chr16:67464092-67464321 | Common:1; Rare:48 | ||||
chr16:67845364-67845509 | Common:2; Rare:20 | ||||
chr16:67845560-67845630 | Rare:16 |