chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167607579167607579T41GENIChomozygous141487962
3167607919167607920TC28GENIChomozygous141572420
3167607984167607985AG32GENIChomozygous141572421
3167608080167608081GA36GENIChomozygous141572422
3167608598167608599AG50GENIChomozygous141572423
3167608605167608605CTGTCTGTTG50GENIChomozygous141487963
3167610655167610656CT36GENIChomozygous141572424
3167610845167610846TA3GENIChomozygous144655369
3167610794167610795T22GENIChomozygous143006167
3167610833167610834TA3GENIChomozygous143931406
3167610835167610836TA3GENIChomozygous143931407
3167610837167610838TA3GENIChomozygous144655365
3167610839167610840TA3GENIChomozygous144655366
3167610841167610842TA3GENIChomozygous144655367
3167610843167610844TA3GENIChomozygous144655368
3167610849167610850TA3GENIChomozygous144655370
3167611154167611155GA42GENIChomozygous141572425
3167614559167614560GA30GENIChomozygous141572429
3167611669167611670AG52GENIChomozygous141572426
3167612983167612984AG36GENIChomozygous141572427
3167613571167613572CT31GENIChomozygous141572428
3167615770167615771TC15GENIChomozygous141572430
3167617411167617412TC42GENIChomozygous141572431
3167617471167617472TC46GENIChomozygous141572432
3167618003167618004CT54GENIChomozygous141572433
3167622487167622488T44GENICpossibly homozygous141487965