Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:51016940-51017091 | Common:1; Rare:40 | ||||
chr19:51065048-51065155 | Common:1; Rare:33 | ||||
chr19:51311496-51311673 | Common:1; Rare:41 | ||||
chr19:51339713-51340025 | Common:1; Rare:66 | ||||
chr19:51366269-51366588 | Common:8; Rare:99; Clinvar (benign):2 | ||||
chr19:51367486-51367842 | Common:2; Rare:102 | ||||
chr19:51390508-51390652 | Common:1; Rare:49 | ||||
chr19:51571167-51571433 | Common:5; Rare:72 | ||||
chr19:51887848-51888120 | Rare:95 | ||||
chr19:51926731-51926805 | Common:1; Rare:16 | ||||
chr19:51927406-51927522 | Common:1; Rare:31 | ||||
chr19:51986788-51987012 | Common:1; Rare:60 | ||||
chr19:52008130-52008312 | Rare:55 | ||||
chr19:52027793-52028066 | Common:1; Rare:43 | ||||
chr19:52028325-52028503 | Common:3; Rare:40 |