Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:31846596-31846788 | Rare:59 | ||||
chr13:35475423-35475668 | Rare:77 | ||||
chr13:48413111-48413193 | Rare:11 | ||||
chr13:52194416-52194487 | Rare:17 | ||||
chr13:109272038-109272210 | Common:5; Rare:42 | ||||
chr14:49633956-49634053 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49853807-49854043 | Rare:46 | ||||
chr14:49862265-49862558 | Common:1; Rare:64 | ||||
chr14:49862666-49863039 | Common:1; Rare:171 | ||||
chr14:61547525-61547651 | Common:3; Rare:24 | ||||
chr14:61570651-61570673 | Rare:7 | ||||
chr14:72665421-72665679 | Common:4; Rare:46 | ||||
chr14:81219345-81219504 | Rare:35 | ||||
chr14:100825971-100826160 | Rare:41 | ||||
chr15:39195975-39196291 | Rare:73 |