chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148902053389020534TTGC4GENICheterozygous49575858
148902207889022079CCCA18GENIChomozygous48824767
148902298989022991AC--4GENICheterozygous48824769
148902445989024460TTCTCTC10GENICheterozygous49317205
148902675389026755TG--7GENICheterozygous49413341
148903436489034365CCATCTATCT9GENICpossibly homozygous48824783
148903436489034365CCATCT9GENICheterozygous49425059
148903525289035256AAAA----12GENICheterozygous49028364
148903525589035256A-12GENICheterozygous49372427
148904008989040090CCA5GENICheterozygous48824787
148904686989046870G-19GENIChomozygous48824789
148904783489047835AAAGAGAG10GENICheterozygous49317208
148904948889049489GGCA3GENIChomozygous48824793
148903709789037098T-10GENIChomozygous49484288
148904874189048742CA15GENIChomozygous49484289