chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13107699602107699602A51GENICheterozygous129094582
13107704821107704821T38GENICheterozygous129094583
13107787579107787580GC8GENICheterozygous134444836
13107787585107787586AG9GENICheterozygous134444837
13107787608107787609TG9GENICpossibly homozygous118468078
13107787614107787615TG11GENICpossibly homozygous118468079
13107787626107787627TG10GENICpossibly homozygous114859110
13107871275107871278AGA61GENICheterozygous129094584