chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4162613467162613468AG18GENIChomozygous57004686
4162613652162613653GA16GENIChomozygous57004687
4162613653162613654CA16GENIChomozygous57004688
4162614485162614486GA27GENIChomozygous57004689
4162614498162614499CCG33GENIChomozygous57004690
4162614499162614500AAGG32GENIChomozygous57004692
4162614525162614526AG34GENIChomozygous57004693
4162614799162614800AC23GENIChomozygous57004694
4162615093162615094GA23GENIChomozygous57004695
4162615824162615826TT--15GENIChomozygous57546233
4162615853162615854TTTTTG18GENICheterozygous57004697
4162615942162615943TC20GENIChomozygous57004698
4162616434162616435AG22GENIChomozygous57004699