chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89694022296940223TC31GENIChomozygous52745589
89694023596940236GA38GENIChomozygous52745590
89694181796941818CT36GENIChomozygous52745591
89694226196942262AT19GENIChomozygous52745592
89694234696942347GGTT19GENIChomozygous52745593
89694279896942799TG35GENIChomozygous52745594
89694311096943111TTA31GENIChomozygous52745595
89694355996943560CT22GENIChomozygous52745596
89694381696943817CT24GENICpossibly homozygous52745597
89694385596943856CT26GENIChomozygous52745598
89694385696943857AG26GENIChomozygous52745599
89694403496944036CC--12GENIChomozygous52745600
89694456796944568TC22GENICheterozygous53288709
89694458196944584ATC---13GENICpossibly homozygous52745601
89694638396946384AG38GENIChomozygous52745602
89694667796946678CT28GENIChomozygous52745603
89694791696947918TC--22GENICpossibly homozygous52745604
89694846096948461TC31GENIChomozygous52745605
89694851896948519GGA20GENICpossibly homozygous52745606
89695098596950986GGTGGT29GENIChomozygous52745607
89695105996951060GA54GENIChomozygous52745608
89695125796951258CT45GENIChomozygous52745609
89695216696952167GA34GENICpossibly homozygous52745610
89695234296952343CCG51GENIChomozygous52745611
89695477896954779AG44GENICpossibly homozygous52745612
89695580796955810AAC---17GENIChomozygous52745613
89695619796956198T-5GENIChomozygous52745614
89695624596956246AC9GENIChomozygous52745615
89695640496956405T-18GENIChomozygous52745616
89695788796957929TAGCAAGACCCCCTCATAAGATCCCAGGTCCCAACGAGTCTG------------------------------------------9GENIChomozygous52745617
89695838896958389CG29GENIChomozygous52745618