chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101168408101168410AA--23GENIChomozygous52936166
10101168904101168905CA24GENICpossibly homozygous51580645
10101170306101170307G-6GENIChomozygous51580651
10101170719101170720AG29GENIChomozygous51580655
10101170940101170941TC39GENIChomozygous51580657
10101173083101173084GT14GENIChomozygous51580665
10101173971101173972CT32GENIChomozygous52936168
10101174152101174153TC22GENIChomozygous51580667
10101174374101174375CT27GENIChomozygous52936171
10101175299101175300CT19GENIChomozygous51580669
10101175468101175469GC20GENIChomozygous52936173
10101175478101175479GA17GENIChomozygous52936175
10101171878101171880AC--4GENICheterozygous52969045