chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728380217283803TG21GENIChomozygous113361795
141728481617284817CT22GENIChomozygous113361797
141728489917284900CT21GENIChomozygous113361799
141728505217285053TA15GENIChomozygous113361801
141728505817285059CT12GENIChomozygous113361803
141728520317285204GC23GENIChomozygous113361805
141728563217285633CT27GENIChomozygous113361809
141728587617285877CG12GENIChomozygous113361811
141728588117285882CT10GENIChomozygous113361813
141728645617286457TC19GENIChomozygous113361815
141728669517286696CT17GENIChomozygous113361817
141728676817286769TA13GENIChomozygous113361819
141728677617286777TC5GENIChomozygous113361821
141728685817286859TC10GENIChomozygous113361824
141728703617287037CA14GENIChomozygous113361826
141728751117287512TC8GENIChomozygous113577803
141729061517290616GT6GENIChomozygous118801398
141729113417291135GA23GENIChomozygous113361832
141729148217291483GC22GENIChomozygous113361834
141729201917292020CT24GENIChomozygous113361836
141729228617292287GC24GENIChomozygous113361838
141729295017292951CT18GENIChomozygous113361840
141729299117292992TC16GENICheterozygous113361842
141729314017293141GA26GENIChomozygous113361844
141729327917293280AC14GENIChomozygous113361846
141729329117293292TC14GENIChomozygous113361848
141729472117294722AG20GENIChomozygous113361852
141729490717294908AG10GENIChomozygous113361854
141729502417295025TC13GENIChomozygous113361856
141729540917295410CT18GENIChomozygous113361858
141729542117295422GA19GENIChomozygous113361860
141729553717295538TC15GENIChomozygous113361862
141729593717295938AG7GENIChomozygous113361866
141729638517296386AG32GENIChomozygous113361868
141729972117299722AG20GENIChomozygous113361870
141730108917301090TG30GENIChomozygous113361872
141730127317301274TC22GENIChomozygous113361874
141728604017286041GA16GENIChomozygous113720565