chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152375206152375207CT22GENIChomozygous55927982
5152375740152375741GA32GENIChomozygous55927984
5152375891152375892AG17GENIChomozygous55927986
5152376857152376858GC29GENIChomozygous55927988
5152377429152377430CT22GENIChomozygous55927990
5152377485152377486GC19GENIChomozygous55927992
5152377596152377597GGTT15GENIChomozygous55927994
5152377714152377715AG23GENIChomozygous55927996
5152377880152377881CA32GENIChomozygous55927998
5152378049152378058TTTTTTTTT---------7GENIChomozygous55928000
5152378265152378266AG17GENIChomozygous55928002
5152378611152378612GT12GENIChomozygous55798866
5152378613152378614GC13GENIChomozygous55798867
5152378615152378616GC13GENIChomozygous55798868
5152378616152378617GA13GENIChomozygous55798869
5152378621152378622GC13GENIChomozygous55798870
5152378630152378631AACAC9GENIChomozygous55928004
5152378676152378677AT17GENIChomozygous55928006
5152378764152378769AAAAA-----3GENIChomozygous55928008
5152378955152378956A-11GENIChomozygous55928010
5152383158152383159CCGCAGGGGAGACAGTTCACACCGCACCCAAGTGAATGT24GENIChomozygous56356581
5152383576152383578AA--9GENICheterozygous56461164
5152383577152383578A-9GENICpossibly homozygous56356583