chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4164943961164943962TTCA9GENICheterozygous57351770
4164944181164944182TC76GENIChomozygous57009616
4164944262164944263TG73GENIChomozygous57009617
4164944485164944486TG54GENICpossibly homozygous57009618
4164944765164944766CCTG58GENIChomozygous57009619
4164945796164945797TC53GENIChomozygous57009620
4164946211164946212GT44GENIChomozygous57009621
4164946500164946501CT43GENIChomozygous57009622
4164946591164946592AG53GENIChomozygous57009623