chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117003570070035700TA26GENIChomozygous133246428
117003574870035749CA17GENIChomozygous115897427
117003580870035809TC25GENIChomozygous115897429
117003591270035913A53GENIChomozygous128920720
117003635770036358TC55GENIChomozygous115897431
117003687770036877A37GENICpossibly homozygous128920721
117003702570037026GA59GENIChomozygous115897433
117003757770037578CT54GENIChomozygous115897435
117003901670039017AC15GENIChomozygous115897437
117003901870039019AG18GENIChomozygous115897439
117003908470039085TG40GENIChomozygous116223549
117003862370038624GA59GENIChomozygous116160875
117003882370038824AT74GENIChomozygous116223541
117003912370039123G54GENIChomozygous133246429
117003926170039262TC55GENIChomozygous116160877
117003933370039334AG54GENIChomozygous116160879
117003989270039893AG53GENIChomozygous116160881
117004064270040643TC35GENIChomozygous116160887
117004017670040177GA44GENIChomozygous115897441
117004033270040333GA50GENIChomozygous116160883
117004034070040341GA55GENIChomozygous116160885
117004086070040861CT53GENIChomozygous116160889
117004103170041032TA47GENIChomozygous116160891
117004154470041557CAGTTGAGCATTT44GENIChomozygous133246430
117004164370041643TCT12GENIChomozygous128920723
117004174670041747TG32GENIChomozygous116160893
117004212270042123AG49GENIChomozygous116160895
117004213870042139CG49GENIChomozygous115897447
117004249070042491TC58GENIChomozygous116160897
117004251670042517TC57GENIChomozygous116160899
117004253170042532GA54GENIChomozygous116160901
117004266470042665CT57GENIChomozygous116160903
117004274170042742GA61GENIChomozygous116160905
117004301970043020CT60GENIChomozygous116160907
117004305570043056GA62GENIChomozygous116160909
117004342670043427CG57GENIChomozygous116160911
117004353670043537CT55GENIChomozygous116160913
117004365170043652CG53GENIChomozygous116160915
117004393670043937TC59GENIChomozygous115897449
117004450770044508TC64GENIChomozygous115897451
117004195370041954GT29GENIChomozygous118163656