chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832057478320575AG20GENIChomozygous811759054
47832062078320621AC19GENIChomozygous811759055
47832063878320639CA21GENIChomozygous811759056
47832081578320816GA19GENIChomozygous811759057
47832140078321401TC31GENIChomozygous811759058
47832144778321448TA27GENIChomozygous811759059
47832274678322747CA29GENIChomozygous811759060
47832291378322914TA39GENIChomozygous811759061
47832291878322919CA41GENIChomozygous811759062
47832306478323065CT34GENIChomozygous811759063
47832315378323154GA30GENIChomozygous811759064
47832367778323678GA12GENIChomozygous811759065
47832382878323829TC11GENIChomozygous811759066
47832399678323997GA19GENIChomozygous811759067
47832419778324198CT22GENIChomozygous811759068
47832429778324298CT19GENIChomozygous811759069
47832433978324340GT23GENIChomozygous811759070
47832469278324693TA30GENIChomozygous811759071
47832473778324738GC37GENIChomozygous811759072
47832505378325054AG24GENIChomozygous811759073
47832524978325250CT20GENIChomozygous811759074
47832595578325956AG34GENIChomozygous811759075
47832653078326531AG33GENIChomozygous811759076
47832659078326591AG31GENIChomozygous811759077
47832682978326830TC25GENIChomozygous811759078
47832691478326915AG24GENIChomozygous811759079
47832703778327038TC17GENIChomozygous811759080