chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115975732115975733TG69GENICheterozygous54072530
7115975735115975736GC66GENICheterozygous54072532
7115975738115975739TG69GENICheterozygous54831703
7115975745115975746CT69GENICheterozygous54831705
7115975749115975750TA73GENICheterozygous54831707
7115975772115975773AG84GENICheterozygous54072534
7115975885115975886GA73GENICheterozygous54831709
7115975894115975895CA73GENICheterozygous54831711
7115975896115975897GA74GENICheterozygous54831713
7115975927115975928AT69GENICheterozygous54072538
7115975942115975943CA67GENICheterozygous54072540
7115975946115975947CT65GENICheterozygous54072542
7115975973115975974AG66GENICheterozygous54072544
7115976050115976051TC44GENICheterozygous54072546
7115976092115976093CT31GENICpossibly homozygous54831715
7115976105115976106TC28GENIChomozygous54231103
7115976507115976508GA68GENICheterozygous54231107
7115976514115976515TA66GENICheterozygous54231109
7115976577115976578AC68GENICheterozygous54072550
7115976588115976589AG67GENICheterozygous54072552
7115976615115976616GA75GENICheterozygous54072554
7115976774115976775TC66GENIChomozygous54072560
7115976795115976796CT54GENICpossibly homozygous54831717
7115976827115976828GT49GENIChomozygous54831719
7115977049115977050AC59GENIChomozygous54072564
7115977269115977270CT27GENIChomozygous54831721
7115977824115977825TG41GENIChomozygous54072566
7115977936115977937TG25GENICpossibly homozygous54831723
7115976368115976369TC6GENICheterozygous54586753