chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119174141891741419GC35GENIChomozygous50866865
119174192291741923AAT21GENICpossibly homozygous50866874
119174192291741923AATT21GENICheterozygous50866875
119174214391742144A-17GENIChomozygous50866876
119174264191742642TC16GENIChomozygous50866877
119174264691742647AG21GENIChomozygous50866878
119174274591742746GA29GENIChomozygous50866879
119174303091743031CT25GENIChomozygous50866880