chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18398044383980444GA66GENIChomozygous108879798
18398079983980800AG93GENIChomozygous108879799
18398119183981192CG73GENIChomozygous109305010
18398173883981739AG54GENIChomozygous108879801
18398332283983323CT39GENIChomozygous109305012
18398353183983532TC58GENIChomozygous108879802
18398498083984981AG93GENICpossibly homozygous108879804
18398539183985392AG78GENIChomozygous108879806
18398552283985523TA76GENIChomozygous108879807
18398608983986090CT18GENIChomozygous120820255
18398671183986712GC67GENIChomozygous109305016
18398924083989241TC38GENIChomozygous108879809
18398980183989802CG44GENIChomozygous109305026
18399051883990519CT40GENIChomozygous120820258
18398255983982560CT55GENIChomozygous120482426
18398593083985931GC46GENIChomozygous120482427
18398625983986260GA34GENIChomozygous120482428
18398878883988789CT61GENIChomozygous120482429
18398983883989839TC57GENIChomozygous120482430
18399067183990672CT40GENIChomozygous120482431
18398729683987302CCCTCT42GENIChomozygous134387575
18398764983987649TCCC7GENIChomozygous134387576
18398825883988258A36GENIChomozygous134387577
18398826783988267TT36GENIChomozygous134387578