chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118051469118051470A-14GENIChomozygous54667090
6118051851118051852TC19GENIChomozygous54667092
6118051853118051854TG19GENIChomozygous54667094
6118051854118051855GGT19GENIChomozygous54667096
6118051860118051861AAG19GENIChomozygous54667098
6118051862118051863AAT19GENIChomozygous54667100
6118052059118052060GGTTTAGTCCAGGA18GENIChomozygous54667102
6118052968118052969T-7GENIChomozygous54667110
6118052971118052974ACC---6GENIChomozygous54667112
6118052957118052958GGGATTTA7GENIChomozygous55532923
6118052960118052961TTCAGTGGTAGAGCGCTTG5GENIChomozygous55532925
6118052975118052976TA5GENIChomozygous55532927