chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4116928349116928350CT11GENIChomozygous71110287
4116928371116928372TC13GENIChomozygous71110291
4116928381116928382AC17GENIChomozygous71110295
4116928393116928394GC17GENIChomozygous71110299
4116928409116928410AC32GENIChomozygous71110304
4116928435116928436CT31GENIChomozygous71110309
4116928445116928446AC20GENIChomozygous71110313
4116928446116928447GT21GENIChomozygous71110318
4116928452116928453GA24GENIChomozygous71110322
4116928518116928519GC42GENIChomozygous71110326
4116941721116941722AT50GENICheterozygous72271537
4116958807116958808CA43GENICheterozygous72271539
4116963142116963143TC35GENIChomozygous71110484
4116963153116963154CA31GENIChomozygous71110488
4116974171116974172GA20GENIChomozygous71110558
4116974172116974173TA18GENIChomozygous71110562
4116974181116974182CA17GENIChomozygous71110566
4116974185116974186GA15GENICpossibly homozygous71110570
4116974187116974188CA14GENICpossibly homozygous71110574
4116974189116974190GA15GENIChomozygous71110577
4116974209116974210TA17GENIChomozygous71110581
4116975129116975130GA35GENICheterozygous72271541