chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109389134109389135CT33GENIChomozygous51599138
10109391046109391047TC63GENIChomozygous51599139
10109391914109391915GA32GENIChomozygous51599140
10109392071109392073CA--26GENIChomozygous51599142
10109392097109392098CT19GENICpossibly homozygous51599143
10109393080109393081T-14GENIChomozygous51599150
10109393643109393645TT--52GENIChomozygous51599151
10109393846109393847TC47GENIChomozygous51599152
10109394076109394077GA17GENIChomozygous51599153
10109394100109394101CCT5GENICheterozygous51599154
10109394100109394101CCTT5GENICheterozygous51599155
10109394149109394150AAT23GENIChomozygous51599156
10109394629109394630CT15GENIChomozygous51599157
10109394684109394685CCTTTTTT1GENIChomozygous52734672
10109394854109394855TC16GENIChomozygous51599160
10109394981109394982TC22GENIChomozygous51599161