chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117003574870035749CA19GENICpossibly homozygous115897427
117003580870035809TC37GENIChomozygous115897429
117003635770036358TC40GENIChomozygous115897431
117003702570037026GA58GENIChomozygous115897433
117003757770037578CT44GENIChomozygous115897435
117003862370038624GA56GENIChomozygous116160875
117003882370038824AT52GENIChomozygous116223541
117003901670039017AC25GENIChomozygous115897437
117003901870039019AG29GENIChomozygous115897439
117003908470039085TG43GENIChomozygous116223549
117003926170039262TC38GENIChomozygous116160877
117003933370039334AG34GENIChomozygous116160879
117003989270039893AG45GENIChomozygous116160881
117004017670040177GA54GENIChomozygous115897441
117004033270040333GA48GENIChomozygous116160883
117004034070040341GA46GENIChomozygous116160885
117004064270040643TC50GENIChomozygous116160887
117004086070040861CT61GENIChomozygous116160889
117004103170041032TA28GENIChomozygous116160891
117004174670041747TG34GENIChomozygous116160893
117004195370041954GT27GENIChomozygous118163656
117004212270042123AG63GENIChomozygous116160895
117004213870042139CG62GENIChomozygous115897447
117004249070042491TC51GENIChomozygous116160897
117004251670042517TC45GENIChomozygous116160899
117004253170042532GA44GENIChomozygous116160901
117004266470042665CT52GENIChomozygous116160903
117004274170042742GA53GENIChomozygous116160905
117004301970043020CT61GENIChomozygous116160907
117004305570043056GA70GENICpossibly homozygous116160909
117004342670043427CG42GENIChomozygous116160911
117004353670043537CT50GENIChomozygous116160913
117004365170043652CG42GENIChomozygous116160915
117004393670043937TC60GENIChomozygous115897449
117004450770044508TC48GENICpossibly homozygous115897451