chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152375206152375207CT53GENIChomozygous55927982
5152375740152375741GA58GENICpossibly homozygous55927984
5152375891152375892AG41GENIChomozygous55927986
5152376857152376858GC57GENIChomozygous55927988
5152377429152377430CT42GENIChomozygous55927990
5152377485152377486GC45GENIChomozygous55927992
5152377596152377597GGTT46GENIChomozygous55927994
5152377714152377715AG56GENICpossibly homozygous55927996
5152377880152377881CA48GENIChomozygous55927998
5152378049152378058TTTTTTTTT---------1GENIChomozygous55928000
5152378265152378266AG74GENIChomozygous55928002
5152378611152378612GT21GENIChomozygous55798866
5152378613152378614GC21GENIChomozygous55798867
5152378615152378616GC21GENIChomozygous55798868
5152378616152378617GA20GENIChomozygous55798869
5152378621152378622GC29GENIChomozygous55798870
5152378630152378631AACAC11GENIChomozygous55928004
5152378676152378677AT30GENIChomozygous55928006
5152378764152378769AAAAA-----4GENICheterozygous55928008
5152378788152378789TG22GENICheterozygous55798871
5152378955152378956A-27GENIChomozygous55928010
5152379002152379006ACAC----1GENIChomozygous55798872
5152383148152383149GC37GENICheterozygous55928012
5152383150152383151GA39GENICheterozygous55928013
5152383156152383157CT43GENICheterozygous55928015
5152383158152383159CT42GENICheterozygous55928017
5152383188152383189G-33GENICheterozygous55928019
5152383576152383577A-3GENIChomozygous55928021