chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101556444101556445TC57GENIChomozygous113941749
5101557688101557689GA62GENIChomozygous113941751
5101558635101558636AG44GENIChomozygous113941753
5101559558101559559CT57GENICpossibly homozygous113941755
5101563819101563820A48GENIChomozygous128218256
5101568713101568714AC52GENIChomozygous113941757
5101571224101571225GA64GENIChomozygous113941759
5101574084101574085CT48GENIChomozygous113941761
5101584519101584519T27GENIChomozygous128218261
5101565326101565326G46GENIChomozygous128218257
5101568227101568228A55GENIChomozygous128218258
5101574332101574336TCAG42GENIChomozygous128218259
5101574872101574872ATAG68GENIChomozygous128218260
5101581421101581424TGA1GENIChomozygous133399214
5101581427101581429GT1GENIChomozygous133399215
5101585232101585233AG33GENIChomozygous113941763
5101585371101585372GA35GENIChomozygous113941765
5101587363101587365TC62GENIChomozygous128218262