chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25850995258509953CA9GENIChomozygous990064891
25851033758510338AT19GENIChomozygous990064892
25851035758510358TC17GENIChomozygous990064893
25851092158510922CG30GENIChomozygous990064894
25851181958511820AC18GENIChomozygous990064895
25851263358512634GA19GENIChomozygous990064896
25851479858514799GA28GENIChomozygous990064897
25851568258515683CT22GENIChomozygous990064898
25851894158518942GA16GENIChomozygous990064899
25851976458519765TC21GENIChomozygous990064900
25851984858519849TA24GENIChomozygous990064901
25852005158520052CT25GENIChomozygous990064902
25852071858520719CT19GENIChomozygous990064903
25852278258522783GA25GENIChomozygous990064904
25852293458522935CT20GENIChomozygous990064905
25852305158523052TC34GENIChomozygous990064906
25852654058526541CT31GENIChomozygous990064907
25853184058531841TC17GENIChomozygous990064908
25853188358531884TC23GENIChomozygous990064909
25853326758533268GA27GENIChomozygous990064910