chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119174141891741419GC33GENICpossibly homozygous50866865
119174151491741526TGCAGTGCTATA------------18GENIChomozygous50866868
119174192291741923AAT19GENIChomozygous50866874
119174264191742642TC29GENIChomozygous50866877
119174264691742647AG27GENIChomozygous50866878
119174303091743031CT21GENICpossibly homozygous50866880
119174199891741999GT13GENIChomozygous50975589
119174215391742154AC14GENIChomozygous50975590