Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24922795-24922995 | Rare:57; Clinvar:1 | ||||
chr13:25301502-25301682 | Common:1; Rare:73 | ||||
chr13:26221791-26221986 | Rare:59 | ||||
chr13:26222243-26222375 | Common:2; Rare:38 | ||||
chr13:27251243-27251647 | Common:6; Rare:122 | ||||
chr13:27424482-27424732 | Common:4; Rare:83 | ||||
chr13:27450130-27450230 | Common:3; Rare:29 | ||||
chr13:27620480-27620790 | Common:2; Rare:102 | ||||
chr13:28658938-28659194 | Rare:108; Clinvar (pathogenic):1 | ||||
chr13:28659591-28659818 | Common:1; Rare:58 | ||||
chr13:30306813-30307187 | Common:7; Rare:99 | ||||
chr13:30307376-30307596 | Common:2; Rare:76 | ||||
chr13:30465795-30466134 | Common:1; Rare:107 | ||||
chr13:30617287-30617392 | Rare:20 | ||||
chr13:30617585-30618000 | Common:1; Rare:127 |