Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:127746719-127746953 | Common:2; Rare:43 | ||||
chr3:128765216-128765498 | Common:1; Rare:36 | ||||
chr3:128822597-128822645 | Common:1; Rare:8 | ||||
chr3:129387773-129387911 | Common:3; Rare:32 | ||||
chr3:129395709-129395778 | Rare:17 | ||||
chr3:129794506-129794670 | Rare:26 | ||||
chr3:130111473-130111707 | Common:3; Rare:61 | ||||
chr3:130991376-130991606 | Rare:42 | ||||
chr3:131361615-131361917 | Common:3; Rare:89 | ||||
chr3:134328253-134328527 | Rare:60 | ||||
chr3:139373258-139373839 | Rare:111; Clinvar (pathogenic):1 | ||||
chr3:141558149-141558166 | Rare:3 | ||||
chr3:141580032-141580055 | Rare:1 | ||||
chr3:141599480-141599591 | Rare:24 | ||||
chr3:141913516-141913727 | Rare:42 |