chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT15GENIChomozygous618818996
7125747342125747343CT11GENIChomozygous618818997
7125747534125747535CT10GENIChomozygous618818998
7125747571125747572GA6GENIChomozygous618818999
7125748329125748330AG20GENIChomozygous618819000
7125748832125748833C-3GENIChomozygous742604472
7125748927125748928GA19GENIChomozygous618819001
7125749012125749013GA19GENIChomozygous618819002
7125749414125749415AG18GENIChomozygous618819003
7125751521125751522AAT11GENICheterozygous742604473
7125751521125751522AATT11GENICheterozygous742604474
7125752000125752001TC15GENIChomozygous618819004
7125752756125752757GA11GENIChomozygous618819005
7125753821125753822CT14GENIChomozygous618819006
7125753897125753898CT16GENIChomozygous618819007
7125753949125753950GA26GENIChomozygous618819008
7125754274125754275AG28GENIChomozygous618819009
7125754320125754321CT24GENIChomozygous618819010
7125754367125754368CT18GENIChomozygous618819011
7125754379125754380GC19GENIChomozygous618819012
7125755157125755158GA6GENIChomozygous618819013
7125755666125755667CT12GENIChomozygous618819014
7125755703125755704CT15GENIChomozygous618819015
7125756500125756501TC12GENIChomozygous618819016
7125756849125756850AG7GENIChomozygous618819017
7125756965125756966GGAAAA5GENICheterozygous742604476
7125756965125756966GGAAAAAAAAAAA5GENICheterozygous742604477
7125757153125757154TTA10GENIChomozygous742604478