chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2119139994119139995GC34GENIChomozygous109994931
2119140160119140161TC31GENIChomozygous109994933
2119141029119141030GA30GENIChomozygous109994935
2119141846119141847TC32GENIChomozygous109994937
2119141855119141856TC36GENIChomozygous109994939
2119142964119142965TG32GENIChomozygous109994941
2119143442119143443TA47GENIChomozygous109994943
2119144693119144694TC40GENIChomozygous109994945
2119145037119145038GT32GENIChomozygous109994947
2119145892119145893TC33GENIChomozygous109994948
2119146227119146228CT35GENIChomozygous109994950
2119146621119146622CT23GENIChomozygous109994952
2119147235119147236CT30GENICpossibly homozygous109994954
2119147659119147660AT28GENICpossibly homozygous109994956
2119147710119147711AT31GENIChomozygous109994958
2119147791119147792AG27GENIChomozygous109994960
2119147904119147905GA34GENIChomozygous109994962
2119148732119148733CT23GENICheterozygous111115607
2119148734119148735CT22GENICheterozygous111115609
2119148735119148736GA21GENICheterozygous111115611
2119148737119148738TC20GENICheterozygous109994964
2119148754119148755CT18GENICheterozygous109994966
2119148946119148947AG5GENIChomozygous109994968
2119150449119150450GA26GENIChomozygous109994970
2119151107119151108CG15GENIChomozygous109994972
2119152021119152022TC25GENIChomozygous109994977
2119152110119152111TC32GENIChomozygous109994979
2119152285119152286CT19GENIChomozygous109994981
2119152410119152411AG37GENIChomozygous109994983