Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:85678703-85678977 | Rare:101 | ||||
chr6:109454247-109454502 | Rare:39 | ||||
chr6:112117746-112118030 | Rare:65; Clinvar:3; Clinvar (benign):4 | ||||
chr6:144286287-144286369 | Rare:20 | ||||
chr6:150683354-150683625 | Common:1; Rare:50 | ||||
chr6:159170047-159170172 | Rare:27 | ||||
chr6:167934535-167934774 | Common:1; Rare:43 | ||||
chr7:149152-149224 | Common:2; Rare:27 | ||||
chr7:15685963-15686028 | Rare:21 | ||||
chr7:15688157-15688426 | Common:2; Rare:76 | ||||
chr7:23285788-23285963 | Common:1; Rare:46 | ||||
chr7:44986602-44986748 | Common:2; Rare:77 | ||||
chr7:45768930-45769141 | Common:1; Rare:61 | ||||
chr7:65750913-65751078 | Common:2; Rare:67 | ||||
chr7:65770728-65770935 | Common:6; Rare:67 |