chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101103462911034630GA18GENIChomozygous148050493
101103464711034647GGAGAGGAACG18GENIChomozygous138668690
101103567411035678TTCT6GENIChomozygous138668691
101103570011035701TA9GENIChomozygous138724623
101103795611037957GA12GENIChomozygous148050494
101103815911038160GA14GENIChomozygous148050495
101104075911040760TC20GENIChomozygous138724628
101104336411043365CT21GENIChomozygous148050496
101104975411049755AG19GENIChomozygous138724634
101105048911050490AT24GENIChomozygous138724635
101105250511052506CT28GENIChomozygous148050497
101105581711055818CT22GENIChomozygous142213528
101105656511056566AG23GENIChomozygous138724638
101106161611061617TC20GENIChomozygous138724640
101106344411063447TCT20GENIChomozygous138668694
101106411111064112TC26GENIChomozygous138724641
101107106511071066A12GENIChomozygous403631673
101104574911045750CA12GENIChomozygous154677513
101107106311071064A12GENIChomozygous403631671
101107106311071064AT12GENICheterozygous403631672
101104574911045750C12GENICheterozygous403276158
101107106511071066AT12GENICheterozygous403631674
101107318911073190CG12GENIChomozygous148050498
101107413311074134CT7GENIChomozygous148050499
101107509911075100AG16GENIChomozygous138724645
101107673711076738TC27GENIChomozygous148050500