chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197638439197638440GA21GENIChomozygous108495376
1197639829197639830TC13GENIChomozygous108495382
1197640271197640272AG35GENIChomozygous108495388
1197641225197641226CT14GENIChomozygous108495390
1197641899197641900TC13GENIChomozygous108495392
1197642489197642490CT18GENIChomozygous108495394
1197643204197643205AC15GENIChomozygous108495398
1197643305197643306GA15GENIChomozygous108495400
1197644037197644038AG16GENIChomozygous108495402
1197645627197645628CT10GENIChomozygous109532164
1197641417197641418AG16GENIChomozygous109532160
1197644557197644558AC11GENIChomozygous109532162
1197645669197645670TC14GENIChomozygous108495408
1197645751197645752AG21GENICpossibly homozygous109532165
1197645994197645995CT43GENICpossibly homozygous109532166
1197647548197647549TC23GENIChomozygous108495422
1197648784197648785TC25GENIChomozygous108495428
1197650081197650082CA23GENIChomozygous109532167
1197650328197650329AG31GENIChomozygous108495436
1197650998197650999TC25GENIChomozygous109532168
1197651442197651443GA7GENIChomozygous109532169
1197652065197652066GA23GENIChomozygous108495450
1197652326197652327TC22GENIChomozygous108495452
1197652375197652376GA33GENIChomozygous109532170
1197654350197654351GA35GENIChomozygous108495464
1197656471197656472CT44GENIChomozygous108495488
1197657325197657326GT36GENIChomozygous109532171
1197657896197657897CT22GENIChomozygous109532172
1197658846197658847TC4GENIChomozygous108495506