chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129795360129795361TC46GENICpossibly homozygous54109587
7129795406129795407A-4GENIChomozygous54241221
7129795965129795966CG6GENIChomozygous54241223
7129795967129795968CA6GENIChomozygous54241225
7129796079129796081GT--18GENICpossibly homozygous54109588
7129796093129796094AT33GENICpossibly homozygous54109589
7129796801129796803CC--27GENICpossibly homozygous54109590
7129796822129796823G-37GENICheterozygous54241227
7129797073129797074GA47GENIChomozygous54109591
7129798576129798577AAAAGC32GENIChomozygous54109592
7129800826129800827CCAT49GENIChomozygous54109594
7129801567129801568G-22GENIChomozygous54109596
7129802532129802533TC44GENIChomozygous54109597
7129803707129803708TA63GENIChomozygous54109598
7129803754129803755AC64GENICpossibly homozygous54109599
7129804462129804465CAC---36GENIChomozygous54109600
7129804464129804466CC--32GENIChomozygous54109601