chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167607579167607579T16GENIChomozygous141487962
3167607919167607920TC10GENIChomozygous141572420
3167607984167607985AG18GENIChomozygous141572421
3167608080167608081GA14GENIChomozygous141572422
3167608598167608599AG16GENIChomozygous141572423
3167608605167608605CTGTCTGTTG15GENIChomozygous141487963
3167610655167610656CT14GENIChomozygous141572424
3167610794167610795T7GENIChomozygous143006167
3167610837167610838TA1GENIChomozygous144655365
3167610839167610840TA1GENIChomozygous144655366
3167610841167610842TA1GENIChomozygous144655367
3167610843167610844TA1GENIChomozygous144655368
3167610845167610846TA1GENIChomozygous144655369
3167610849167610850TA1GENIChomozygous144655370
3167611154167611155GA19GENIChomozygous141572425
3167611669167611670AG22GENIChomozygous141572426
3167610833167610834TA1GENIChomozygous143931406
3167610835167610836TA1GENIChomozygous143931407
3167612983167612984AG25GENIChomozygous141572427
3167613571167613572CT25GENIChomozygous141572428
3167614559167614560GA18GENIChomozygous141572429
3167615770167615771TC8GENIChomozygous141572430
3167617411167617412TC35GENIChomozygous141572431
3167617471167617472TC28GENIChomozygous141572432
3167618003167618004CT29GENICpossibly homozygous141572433
3167622487167622488T29GENIChomozygous141487965
3167614279167614280GA15GENIChomozygous403086008
3167614279167614280G15GENICheterozygous403086007