Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:23979690-23979853 | Common:3; Rare:39 | ||||
chr13:24160517-24160790 | Common:1; Rare:81 | ||||
chr13:24512723-24512856 | Common:3; Rare:38 | ||||
chr13:24922795-24923021 | Rare:69; Clinvar:1 | ||||
chr13:25301455-25301795 | Common:3; Rare:125 | ||||
chr13:26221791-26221982 | Rare:56 | ||||
chr13:26222228-26222323 | Common:3; Rare:27 | ||||
chr13:26557449-26557786 | Common:4; Rare:134 | ||||
chr13:27251225-27251632 | Common:8; Rare:128 | ||||
chr13:27270696-27270830 | Rare:44 | ||||
chr13:27270989-27271207 | Common:2; Rare:71 | ||||
chr13:27450113-27450222 | Common:3; Rare:34 | ||||
chr13:27620596-27620812 | Common:1; Rare:60 | ||||
chr13:28138133-28138229 | Common:1; Rare:30 | ||||
chr13:28659071-28659180 | Rare:47; Clinvar (pathogenic):1 |