chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123154470123154471TC34GENIChomozygous111692027
3123154471123154472GA34GENIChomozygous111692028
3123155170123155171GA29GENIChomozygous111692029
3123155859123155860CT28GENIChomozygous111692030
3123156710123156711GA25GENICpossibly homozygous111692031
3123158857123158858GA35GENIChomozygous111692032
3123158983123158984CT21GENIChomozygous111692033
3123161310123161311CT22GENIChomozygous111692034
3123161460123161461GC23GENIChomozygous111692035
3123162914123162915CT23GENIChomozygous111692036
3123165012123165013GA24GENIChomozygous111692037
3123167440123167441CG15GENIChomozygous111692038
3123168378123168379AT40GENIChomozygous111692039
3123170101123170102CT12GENIChomozygous111692040