chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X105013336105013337AG11GENIChomozygous108527299
X105013440105013441TC6GENIChomozygous108527301
X105015624105015625CG10GENIChomozygous108527303
X105016444105016445CT9GENIChomozygous108527305
X105017155105017156AG11GENICheterozygous120042789
X105018140105018141CT2GENIChomozygous108779489
X105019112105019113AG6GENIChomozygous108527307
X105019852105019853TC11GENIChomozygous108527309
X105022181105022182GA22GENICheterozygous108779491
X105022207105022208TC17GENICheterozygous120042790
X105025416105025417CT3GENIChomozygous108527311
X105026930105026931CG8GENIChomozygous120042791
X105026963105026964TC13GENICheterozygous120042792
X105027856105027857AG7GENICpossibly homozygous108527313
X105028580105028581TC22GENICheterozygous120042793
X105029112105029113AG12GENICheterozygous119942647
X105029133105029134TG13GENICheterozygous119942649
X105031630105031631GA14GENICheterozygous120042794
X105031760105031761AT21GENICheterozygous120042795
X105031856105031857GA17GENICheterozygous120042796
X105031897105031898AG19GENICheterozygous120042797
X105033920105033921AG4GENIChomozygous108527315
X105035994105035995AC10GENIChomozygous108527317
X105036150105036151CT8GENIChomozygous108667238
X105036801105036802TA2GENIChomozygous108779493
X105038651105038652GA19GENIChomozygous108527319