chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162065294620652947GT41GENIChomozygous111753186
162065316020653161TC43GENIChomozygous111753188
162065355220653553CT55GENIChomozygous111753190
162065437120654372TC45GENIChomozygous111948797
162065489320654894AG44GENIChomozygous111753192
162065498820654989TG49GENIChomozygous111948799
162065559620655597CT45GENIChomozygous111753194
162065852320658524GA43GENIChomozygous111753196
162065890220658903AT43GENIChomozygous111753198
162066015920660160AG59GENIChomozygous111753200
162066046520660466TG47GENIChomozygous111753202
162066242520662426CT38GENIChomozygous111753204
162066430820664309GA40GENICpossibly homozygous111753206
162066565720665658TC39GENICpossibly homozygous111753208
162066566520665665GA41GENICpossibly homozygous129340656
162066268520662685AGACAGGGTTTTTCTC40GENIChomozygous129340655