chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113517014835170149TC14GENIChomozygous50728763
113517135435171355A-11GENIChomozygous50728775
113517219235172193TC18GENIChomozygous50728776
113517232435172325CT14GENICpossibly homozygous50728777
113517422935174234TGCCA-----8GENIChomozygous50728778
113517442235174423TG23GENIChomozygous50728779
113517450835174509TC16GENIChomozygous50728780
113517733435177335AG5GENIChomozygous50728782
113517977535179776TC9GENIChomozygous50728786
113518071935180720GA8GENICheterozygous50728787
113518386735183868T-4GENICheterozygous50728794
113518404835184049CA24GENIChomozygous50728795
113518459435184595CT8GENIChomozygous50728796
113518575535185756GA15GENIChomozygous50728797
113518612035186121AT5GENIChomozygous50728798
113518613335186134TA3GENICheterozygous50728799
113518613435186135AG3GENICheterozygous50728800
113518617135186172CT11GENIChomozygous50728801
113518853235188534TC--9GENIChomozygous50728806
113518894335188944TC19GENIChomozygous50728808
113518921235189213AG21GENICpossibly homozygous50728809
113518943235189433TC18GENICpossibly homozygous50728810
113518979735189798GA15GENIChomozygous50728811
113519023535190238GGG---4GENICheterozygous50728812
113519030635190307TC7GENIChomozygous50728813
113519037435190375TG11GENIChomozygous50728814
113519038635190387TTA11GENICheterozygous50728815