chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165516385165516386TC59GENIChomozygous773784901
1165516967165516968CT45GENIChomozygous773784902
1165518186165518187CT38GENIChomozygous773784903
1165518808165518809CT53GENIChomozygous773784904
1165519247165519248GA16GENIChomozygous773784905
1165519564165519565GA23GENIChomozygous773784906
1165519823165519824TC50GENIChomozygous773784907
1165519873165519874CT51GENIChomozygous773784908
1165520032165520033CT50GENIChomozygous773784909
1165520851165520852GA61GENIChomozygous773784910
1165522302165522303GC45GENICheterozygous773784911
1165522304165522305CG43GENICheterozygous773784912
1165522389165522390CT47GENIChomozygous773784913
1165522405165522406CT43GENIChomozygous773784914
1165522406165522407CG42GENIChomozygous773784915
1165523734165523735GT50GENIChomozygous773784916
1165523762165523763CT48GENIChomozygous773784917
1165524310165524311TC30GENIChomozygous773784918
1165525481165525482AC27GENICheterozygous773784919
1165525484165525485CT24GENICheterozygous773784920
1165525629165525630TC50GENIChomozygous773784921
1165525770165525771TC39GENIChomozygous773784922
1165527324165527325CA52GENIChomozygous773784923
1165527481165527482AG51GENIChomozygous773784924
1165527942165527943CT54GENIChomozygous773784925
1165528020165528021CA59GENICpossibly homozygous773784926
1165528136165528137AC31GENICpossibly homozygous773784927
1165528448165528449CG32GENIChomozygous773784928
1165528468165528469TG44GENICpossibly homozygous773784929
1165528554165528555TC55GENIChomozygous773784930
1165528709165528710CG39GENIChomozygous773784931
1165528792165528793AT46GENIChomozygous773784932
1165528959165528960AG49GENIChomozygous773784933
1165529106165529107GA57GENIChomozygous773784934
1165529198165529199CT45GENIChomozygous773784935
1165529444165529445TC6GENIChomozygous773784936
1165529466165529467TG13GENIChomozygous773784937