chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3137651649137651650AG28GENIChomozygous73078167
3137651922137651923TC32GENIChomozygous73078169
3137652614137652615TA20GENIChomozygous73078171
3137652917137652918CT23GENIChomozygous73078174
3137653007137653008CA19GENIChomozygous73078176
3137653027137653028CT17GENIChomozygous73078179
3137653052137653053TC22GENICpossibly homozygous73078181
3137653185137653186TC16GENICpossibly homozygous73078183
3137653248137653249AG26GENICpossibly homozygous73078186
3137653550137653551AG22GENIChomozygous72500697
3137653646137653647CT16GENIChomozygous73078191
3137653763137653764TC17GENIChomozygous73078193
3137653874137653875TA16GENIChomozygous73078195
3137653934137653935GA19GENIChomozygous73078198
3137654337137654338TC26GENIChomozygous72500699
3137654389137654390GA19GENIChomozygous73078200
3137654437137654438GT19GENIChomozygous73078203