Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:131502829-131503004 | Common:1; Rare:80 | ||||
chr3:132659795-132659950 | Common:3; Rare:38 | ||||
chr3:132722137-132722204 | Common:1; Rare:29; Clinvar:5; Clinvar (benign):2 | ||||
chr3:133573837-133573966 | Rare:34 | ||||
chr3:133661856-133662007 | Rare:34 | ||||
chr3:134485437-134485766 | Rare:79 | ||||
chr3:134485966-134486265 | Common:3; Rare:101 | ||||
chr3:135965534-135965785 | Common:1; Rare:109 | ||||
chr3:136752228-136752671 | Common:1; Rare:142 | ||||
chr3:136819019-136819181 | Common:4; Rare:93 | ||||
chr3:136862013-136862306 | Common:1; Rare:92 | ||||
chr3:138329802-138330019 | Common:1; Rare:53 | ||||
chr3:138348378-138348723 | Common:2; Rare:89 | ||||
chr3:138594189-138594460 | Rare:82 | ||||
chr3:138608649-138608937 | Rare:59 |