chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56307001863070019GC21GENICheterozygous56017539
56307186063071861CT23GENICheterozygous55422541
56307187163071872AT18GENICheterozygous55422543
56307194663071947TG17GENICheterozygous55422545
56307272663072727TG24GENICheterozygous55422549
56307291563072916CG30GENICheterozygous55879893
56309161563091616GT27GENICheterozygous55422598
56311322363113224CG10GENICheterozygous55422636
56311325163113252CT7GENIChomozygous55422638
56311619363116194GA46GENICheterozygous55422650
56311781663117817GA37GENICheterozygous55422652
56311786663117867CT41GENICheterozygous56017542
56311786763117868AG41GENICheterozygous55422654
56311789463117895TC42GENICheterozygous55422656
56311798363117984AG37GENICheterozygous55422658
56311800963118010TC36GENICheterozygous55422660
56311801063118011GA36GENICheterozygous55422662
56311801863118019CT32GENICheterozygous55422664
56311802463118025CG32GENICheterozygous55422666
56311803963118040C-30GENICheterozygous55422668
56311807463118075TC18GENICheterozygous55422670
56311807763118078GT19GENICheterozygous55422672
56311808663118087TA17GENICheterozygous55422674