chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162140321021403211CG21GENIChomozygous111754650
162140360821403609TC32GENIChomozygous111754654
162140475221404753GA21GENIChomozygous111754656
162140491421404915AG29GENIChomozygous111949345
162140491821404919GA30GENIChomozygous112053187
162140540621405407CT24GENIChomozygous111754658
162140583521405836TA32GENIChomozygous111754660
162140585021405851TA31GENIChomozygous111754662
162140589921405900AG23GENIChomozygous111754664
162140619721406198AG27GENIChomozygous111754666
162140637421406375CT27GENIChomozygous111754668
162140678621406787TA22GENIChomozygous111754670
162140693521406936TC30GENIChomozygous111754672
162140771621407717TA9GENIChomozygous111754674
162140800221408003AG14GENIChomozygous111754676
162140859821408599AG34GENIChomozygous111754678
162140879321408794TA27GENIChomozygous111754680
162140935821409359CG21GENIChomozygous111754682
162141504221415043TC28GENIChomozygous111754684
162142007321420074AG27GENIChomozygous112053192
162142082721420828CT43GENIChomozygous112053193
162142150321421504TC26GENIChomozygous112053194
162142443621424437AG24GENIChomozygous112250731
162142453421424535AG41GENIChomozygous112053198
162142097721420978CT28GENIChomozygous112401107
162142341721423418CT19GENICpossibly homozygous112401108