chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187669225187669226CT29GENIChomozygous110167672
2187670032187670033TA22GENIChomozygous110167673
2187670134187670135AC21GENIChomozygous111278289
2187670135187670136AT21GENIChomozygous111278291
2187671022187671023TC15GENIChomozygous110803930
2187671113187671114GA14GENIChomozygous110803931
2187672236187672237AG22GENIChomozygous110167674
2187675706187675707TC16GENIChomozygous111278295
2187676747187676748AT19GENIChomozygous110803934
2187676773187676774CT23GENIChomozygous110803935
2187678421187678422CT22GENIChomozygous111278299
2187678863187678864CA15GENIChomozygous111278301
2187679063187679064AG26GENIChomozygous111278303
2187679230187679231AG20GENIChomozygous110803936
2187679265187679266GA25GENIChomozygous111278304
2187680714187680715AC12GENIChomozygous110803938
2187680823187680824TA11GENICheterozygous110803940
2187680853187680854TC10GENIChomozygous110803941
2187680854187680855TC10GENIChomozygous110993162
2187681076187681077TC17GENIChomozygous111278306
2187681801187681802GA18GENIChomozygous111278308
2187681809187681810GA24GENIChomozygous111278310
2187682404187682405AC19GENIChomozygous110167698
2187683166187683167TC13GENIChomozygous110167699
2187684327187684328GA13GENIChomozygous111278312
2187684962187684963AG24GENIChomozygous111278314
2187685754187685755TC17GENIChomozygous110803944
2187686505187686506AG17GENIChomozygous110167702
2187686516187686517TA17GENIChomozygous111278320
2187686979187686980TG8GENIChomozygous110803945
2187687155187687156TA13GENIChomozygous110803947
2187688864187688865GC16GENIChomozygous111278322
2187689018187689019CT22GENIChomozygous111278324
2187689377187689378AC27GENIChomozygous110803949
2187689410187689411AG22GENIChomozygous110167703
2187690834187690835TC12GENIChomozygous110167704
2187690911187690912GA24GENICpossibly homozygous111278326
2187691277187691278TC20GENIChomozygous110167705
2187692571187692572AT16GENIChomozygous111278328
2187692573187692574AT16GENIChomozygous110167706