Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:21176484-21176704 | Common:2; Rare:97 | ||||
chr13:21604127-21604260 | Common:3; Rare:70 | ||||
chr13:23570549-23570748 | Common:2; Rare:37 | ||||
chr13:23889270-23889586 | Common:1; Rare:106 | ||||
chr13:24512722-24512842 | Common:3; Rare:34 | ||||
chr13:24922810-24923032 | Common:1; Rare:66; Clinvar:1 | ||||
chr13:26221782-26221912 | Rare:34 | ||||
chr13:27171774-27171876 | Rare:34 | ||||
chr13:27251265-27251623 | Common:4; Rare:103 | ||||
chr13:27270680-27270830 | Rare:49 | ||||
chr13:27450124-27450232 | Common:3; Rare:32 | ||||
chr13:27620544-27620743 | Common:1; Rare:57 | ||||
chr13:28138470-28138561 | Common:1; Rare:21 | ||||
chr13:28658922-28659001 | Rare:19 | ||||
chr13:28659081-28659184 | Rare:45; Clinvar (pathogenic):1 |