chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102136370102136371CT34GENICpossibly homozygous116712598
10102136379102136380CG36GENIChomozygous116712600
10102136651102136652GA29GENIChomozygous116712602
10102136666102136667TC47GENIChomozygous116712604
10102138186102138187CG49GENIChomozygous116712606
10102138273102138274CT55GENIChomozygous116712608
10102138431102138432CA65GENIChomozygous116712610
10102138625102138626CG44GENIChomozygous116712612
10102138627102138628GA45GENIChomozygous116712614
10102138634102138635GC47GENICpossibly homozygous116712616
10102138638102138639GA46GENIChomozygous116712618
10102138849102138850GA57GENIChomozygous116712620
10102138973102138974CT55GENIChomozygous116712622
10102139399102139400GA37GENIChomozygous116712624
10102139536102139537AG19GENICheterozygous118011883
10102140833102140834TC32GENICpossibly homozygous116712626
10102140843102140844AC39GENIChomozygous116712628
10102141065102141066AT88GENICheterozygous118052487
10102141075102141076CT102GENICheterozygous118052488
10102141161102141162CG68GENICheterozygous118011884
10102141171102141172CA64GENICheterozygous118052489
10102141381102141382CT67GENICheterozygous118011885
10102141392102141393GA49GENICheterozygous118011886
10102141395102141396AT49GENICheterozygous118011887
10102140973102140974TG53GENICheterozygous117232363
10102139706102139707GT13GENICheterozygous116958828