chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1282142514282142515AT16GENIChomozygous108670827
1282144368282144369GA22GENIChomozygous108670828
1282144486282144487AC24GENIChomozygous108670829
1282144863282144864AG19GENIChomozygous108670830
1282145149282145151AC24GENIChomozygous127519553
1282145471282145472AT20GENIChomozygous108670831
1282148607282148608GA17GENIChomozygous108670832
1282149577282149577T15GENIChomozygous127519554
1282150157282150158TA13GENIChomozygous109386859
1282150641282150642CT20GENIChomozygous108670833
1282151239282151240TC12GENIChomozygous108670834
1282152445282152446AG16GENIChomozygous108670835
1282152616282152617TA20GENIChomozygous108670836
1282152971282152972TC20GENIChomozygous108670837
1282153710282153711TC16GENIChomozygous108670838
1282156377282156378AT17GENIChomozygous108670839
1282156443282156444TC15GENIChomozygous108670840
1282157209282157214TAAAA25GENIChomozygous127519555
1282157370282157371AG21GENIChomozygous108670841
1282158694282158695C24GENIChomozygous127519556
1282159086282159092AAAAAT15GENICheterozygous127519557
1282162332282162333CT25GENIChomozygous108670842
1282162800282162801GA21GENIChomozygous108670843
1282163607282163607TTGGATC31GENIChomozygous127519558
1282165523282165524CG12GENIChomozygous108670844
1282166029282166030CG26GENIChomozygous108670845
1282168269282168271AA20GENIChomozygous127519559
1282169058282169059A25GENIChomozygous127519560
1282169541282169542CG32GENIChomozygous108670846