chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2208982295208982296TG24GENIChomozygous110219774
2208985454208985455CA5GENIChomozygous110219776
2208985510208985511AG12GENIChomozygous110219777
2208985511208985512AC12GENIChomozygous110219778
2208986187208986188GA36GENIChomozygous110219779
2208986686208986687CG45GENICheterozygous110219780
2208986694208986695CG42GENICheterozygous110219781
2208986721208986722AG51GENICheterozygous110219782
2208992275208992276GA27GENIChomozygous110219783
2208992650208992651CT38GENICheterozygous111162805
2208988069208988070TC26GENICheterozygous111162799
2208988337208988338AG30GENICheterozygous111162801
2208992643208992644AC36GENICheterozygous111162803
2208992661208992662TG42GENICheterozygous111162807
2208992737208992738AC59GENICheterozygous111162809
2208992838208992839CT47GENICheterozygous110813740
2208992894208992895AG30GENICheterozygous110813744
2208992953208992954GC35GENICheterozygous110813748
2208993045208993046AG25GENICheterozygous110813750
2208993077208993078CT22GENICheterozygous111162810
2208993196208993197GA20GENIChomozygous110219784
2208994713208994714GA15GENIChomozygous110219785
2208999364208999365TG18GENIChomozygous110219786
2209000789209000790TG34GENIChomozygous110219787
2209002188209002189GA19GENIChomozygous110219788
2209003148209003149GT19GENIChomozygous110219789