chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54841868548418686TA52GENIChomozygous113788427
54842056448420565GA79GENICpossibly homozygous113788429
54842087048420871TC47GENIChomozygous113788431
54842088948420890TA50GENICpossibly homozygous113788433
54842095448420955CG47GENICpossibly homozygous113788435
54842097648420977CA49GENIChomozygous113788437
54842108348421084CG49GENICpossibly homozygous113788439
54842153648421537GA51GENIChomozygous113788441
54842153948421540TC51GENIChomozygous113788443
54842171048421711TC39GENIChomozygous113788445
54842226148422262TG89GENICpossibly homozygous113788446
54842262348422624CT50GENIChomozygous113788448
54842292848422929TC61GENIChomozygous113788450
54842546248425463TC75GENIChomozygous113788452
54842660348426604GA56GENIChomozygous113788454
54842666648426667TC62GENIChomozygous113788456
54842910348429104CG45GENICpossibly homozygous113788458
54843122948431230CT75GENIChomozygous113788460
54843150348431504TC43GENIChomozygous113788462
54843259948432600CG52GENICheterozygous113788464
54843270248432703TC50GENIChomozygous113788466
54843491448434915CA57GENICpossibly homozygous113788468
54843503048435031AC136GENICheterozygous113788470
54843504848435049AG128GENICheterozygous113788472
54843607048436071GA57GENIChomozygous113788474
54843653248436533GA38GENIChomozygous113788476