Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46589921-46590055 | Common:1; Rare:15 | ||||
chr13:46656781-46657074 | Rare:37 | ||||
chr13:46795514-46795740 | Rare:37 | ||||
chr13:47955054-47955187 | Rare:30 | ||||
chr13:47996850-47997166 | Common:2; Rare:85; Clinvar (benign):3 | ||||
chr13:48021655-48021915 | Common:2; Rare:44 | ||||
chr13:48057760-48057849 | Rare:15 | ||||
chr13:48060018-48060051 | Rare:6 | ||||
chr13:48089215-48089266 | Common:1; Rare:5 | ||||
chr13:48090343-48090473 | Rare:33 | ||||
chr13:48185833-48186136 | Common:5; Rare:56 | ||||
chr13:48359871-48360018 | Common:1; Rare:36; Clinvar (benign):3 | ||||
chr13:48378532-48378574 | Rare:7 | ||||
chr13:48413031-48413172 | Rare:18 | ||||
chr13:48413248-48413509 | Rare:42 |