chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129795360129795361TC46GENICpossibly homozygous54109587
7129796079129796081GT--14GENIChomozygous54109588
7129796093129796094AT26GENIChomozygous54109589
7129796801129796803CC--32GENICpossibly homozygous54109590
7129797073129797074GA49GENIChomozygous54109591
7129798576129798577AAAAGC35GENIChomozygous54109592
7129798843129798844AC34GENICheterozygous54109593
7129800826129800827CCAT16GENIChomozygous54109594
7129801024129801025CCT24GENICheterozygous54109595
7129801567129801568G-28GENIChomozygous54109596
7129802532129802533TC41GENIChomozygous54109597
7129803707129803708TA69GENIChomozygous54109598
7129803754129803755AC54GENIChomozygous54109599
7129804462129804465CAC---36GENIChomozygous54109600
7129804464129804466CC--32GENIChomozygous54109601