chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152430372152430373CT38GENIChomozygous114543414
5152430964152430965GC47GENICpossibly homozygous114543416
5152431280152431281GA37GENIChomozygous114543418
5152431602152431603GA33GENIChomozygous114543420
5152432612152432613GA14GENIChomozygous114543422
5152432638152432639GA16GENICpossibly homozygous114543424
5152435035152435036AC23GENIChomozygous114543426
5152435037152435038TC23GENIChomozygous114543427
5152436275152436276CT225GENICheterozygous114057223
5152436350152436351CT215GENICheterozygous114057231
5152436426152436427CG206GENICheterozygous114057233
5152436437152436438GA139GENICheterozygous114057235
5152440384152440385CT38GENIChomozygous114057237
5152440449152440450AG30GENIChomozygous114543429