chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105950708959507090CG2GENICheterozygous52319582
105950794659507947CT22GENICpossibly homozygous52062337
105950942459509425TA2GENICheterozygous51897723
105950981259509813CA9GENIChomozygous51465670
105951551859515519CCAA1GENIChomozygous51465678
105951742659517427TC20GENICpossibly homozygous51465681
105952410159524102AG7GENIChomozygous51465688
105952560159525602GT11GENIChomozygous52062339
105952625959526260CA18GENIChomozygous52062341
105952669559526696CT16GENIChomozygous52062343
105952829259528293TC23GENIChomozygous51465689