chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1540354714035472CA27GENIChomozygous113037860
1540357364035737GA32GENIChomozygous113037862
1540375504037551AG19GENIChomozygous112785630
1540394164039417GA25GENIChomozygous113037864
1540396034039604AG16GENIChomozygous113037866
1540403964040397AC25GENIChomozygous113037869
1540410054041006GT29GENIChomozygous113037871
1540410064041007AC29GENIChomozygous113037873
1540425704042571TA29GENIChomozygous113037875
1540434184043419TC20GENIChomozygous113037877
1540450244045025CT24GENIChomozygous113037879
1540459424045943TC27GENIChomozygous112785634
1540464194046420GA13GENIChomozygous113037881
1540491984049199AG27GENIChomozygous112785638
1540501914050192CA21GENIChomozygous113037883
1540503764050377GA32GENIChomozygous113037885
1540518464051847AG15GENIChomozygous113037887
1540527104052711TC23GENIChomozygous113037889
1540528714052872GA23GENIChomozygous113037891
1540546154054616TC18GENIChomozygous113037893
1540560374056038C14GENIChomozygous129225244
1540524984052498GAAG8GENIChomozygous131155247
1540486764048676TATATATATG10GENIChomozygous134242848
1540536944053694G24GENIChomozygous134242849
1540517284051729AG3GENICheterozygous132198195
1540517334051734CA4GENICheterozygous118860338
1540537054053706CT26GENIChomozygous134246302