chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122473847324738474CT6GENIChomozygous50136134
122473882424738825GA5GENIChomozygous50136136
122473893824738939TA1GENIChomozygous50136138
122473896824738969GC1GENIChomozygous50136140
122473910124739102AAT5GENICheterozygous50538660
122473910324739104T-5GENICheterozygous50136144
122473936724739368CCG8GENIChomozygous50136146
122473950424739505CT7GENIChomozygous50136148
122473969124739692CT5GENIChomozygous50136150
122473978724739788GA6GENIChomozygous50136152
122473983624739856CACACACACACACACACACA--------------------2GENICheterozygous50538661
122473983824739856CACACACACACACACACA------------------2GENICheterozygous50538662
122474026624740267A-7GENICheterozygous50538663
122474053324740534TA5GENIChomozygous50136156
122474162724741628GA6GENIChomozygous50136158
122474202324742024AAACAC6GENICheterozygous50136160
122474202324742024AAAC6GENICheterozygous50538664
122474206224742063CCTTTTATTTTT5GENIChomozygous50136162
122474209024742091TC9GENIChomozygous50136164
122474312524743126CCGT2GENIChomozygous50136168