chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109045642109045643AT31GENIChomozygous114937194
6109046188109046189CG44GENIChomozygous114937195
6109046189109046190AG43GENIChomozygous114937196
6109046297109046298AG36GENIChomozygous114937197
6109046364109046365TC49GENIChomozygous114937198
6109046731109046732GA54GENIChomozygous114937199
6109047346109047347GA60GENICpossibly homozygous114937200
6109048588109048589CT36GENICpossibly homozygous114937201
6109049548109049549GA37GENIChomozygous114937202
6109050573109050574GA65GENIChomozygous114937203