chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142062390142062391AG29GENICpossibly homozygous108937327
1142070821142070822TG43GENIChomozygous108937329
1142077757142077758GA48GENIChomozygous109049762
1142063015142063018ACA20GENICpossibly homozygous130823691
1142069830142069830CTC44GENIChomozygous130823692
1142063030142063031CT23GENICheterozygous132001969
1142063225142063226AG15GENIChomozygous108262632
1142073144142073145TC43GENIChomozygous108262640
1142072915142072916TA42GENIChomozygous109049758
1142074106142074107AG31GENIChomozygous109049759
1142077203142077204AG46GENIChomozygous109049760
1142077667142077668CG58GENIChomozygous109049761
1142072107142072108TC41GENIChomozygous130846368
1142082458142082459TC54GENIChomozygous108262646
1142083482142083483TC42GENIChomozygous108262648
1142083492142083493AG44GENIChomozygous108262650