chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5164720727164720728T-2GENICheterozygous56464435
5164720956164720957GGAGGA15GENIChomozygous55830625
5164722325164722326TC20GENICheterozygous55946740
5164722523164722545TCTCTGTCTCTCTGTCTCTGTC----------------------2GENICheterozygous56464436
5164723029164723030AG10GENICheterozygous55830629
5164726584164726585CCG3GENIChomozygous55830634
5164727273164727274CT28GENICpossibly homozygous55830636
5164730623164730635GAGAGAGAGAGG------------5GENICheterozygous56464438
5164732611164732612TG19GENICpossibly homozygous55830640
5164737419164737420TTC1GENIChomozygous55830641
5164737429164737430AAT3GENIChomozygous55830642
5164737574164737575CG29GENICpossibly homozygous55830643
5164737773164737774GGGAAAA1GENIChomozygous55830644
5164738395164738397AA--8GENICheterozygous56464442
5164738396164738397A-8GENICheterozygous56464443
5164738638164738639AAG5GENICheterozygous55830645
5164738680164738681A-1GENIChomozygous55830646
5164740090164740091AG5INTERGENICheterozygous55830647
5164740872164740874AC--8INTERGENICheterozygous55830648
5164741153164741154CA9INTERGENICpossibly homozygous55830649
5164741639164741640GA15INTERGENIChomozygous55830650
5164741640164741641AT15INTERGENIChomozygous55830651
5164742326164742327GA23INTERGENIChomozygous55830652
5164742459164742460CA15INTERGENICpossibly homozygous55830653
5164742979164742980AG10INTERGENICpossibly homozygous55830654
5164743296164743297G-3INTERGENIChomozygous55830660
5164744295164744296GC16INTERGENICpossibly homozygous55830666
5164744437164744438CT27INTERGENIChomozygous55830667
5164744714164744715CT13INTERGENIChomozygous55830668
5164745406164745407GA21INTERGENICpossibly homozygous55830669
5164746985164746986CCAACCAACT9INTERGENICheterozygous55830672