chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168663567886635679TC32GENIChomozygous111895504
168663572886635729CT39GENIChomozygous111895512
168664008386640084GC29GENICheterozygous119211433
168664927886649279AG53GENICheterozygous119229596
168664930286649303AG52GENICheterozygous119229597
168665626086656261AG49GENICpossibly homozygous112038211
168665635386656354AC53GENIChomozygous111895579
168665660686656607AG35GENIChomozygous112038213
168665810886658109CT40GENIChomozygous112038215
168665861186658612GA37GENIChomozygous112038217
168665908186659082TC64GENICheterozygous119242961
168665987786659878TC42GENIChomozygous112038219
168666046586660466CT70GENIChomozygous112038221
168666068486660685AG39GENIChomozygous111895591
168666127386661274AG39GENIChomozygous111895601
168666172686661727TC60GENIChomozygous111895613
168666634286666343AG22GENIChomozygous112332278
168666634586666346TG21GENIChomozygous119136236
168667113786671138CG44GENIChomozygous112038223
168666124386661244AT38GENIChomozygous112180648