chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118051469118051470A-19GENIChomozygous54667090
6118051851118051852TC37GENIChomozygous54667092
6118051853118051854TG36GENIChomozygous54667094
6118051854118051855GGT37GENIChomozygous54667096
6118051860118051861AAG35GENIChomozygous54667098
6118051862118051863AAT33GENIChomozygous54667100
6118052059118052060GGTTTAGTCCAGGA22GENIChomozygous54667102
6118052957118052958GGGATTTA3GENIChomozygous55532923
6118052960118052961TTCAGTGGTAGAGCGCTTG3GENIChomozygous55532925
6118052968118052969T-3GENIChomozygous54667110
6118052971118052974ACC---2GENIChomozygous54667112
6118052975118052976TA2GENIChomozygous55532927
6118053174118053175AG20GENIChomozygous55264357
6118054773118054774AG16GENIChomozygous54960032
6118054878118054879CA27GENIChomozygous54960034
6118055126118055127CG30GENIChomozygous54960036
6118056441118056442TTGTGA44GENIChomozygous54960038
6118056650118056656GTGTGT------17GENICpossibly homozygous55532929