chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134263775042637755GGTTC-----15GENICheterozygous750559709
134263896842638969CT12GENIChomozygous639255502
134263924942639251AG--14GENIChomozygous750559710
134264109342641094TTTGTGTG4GENICheterozygous750559711
134264183742641838AG21GENIChomozygous639255503
134264188642641887TC24GENIChomozygous639255504
134264198642641987G-15GENIChomozygous750559712
134264240542642406TTCTCACA8GENIChomozygous750559713
134264257842642579A-17GENIChomozygous750559715
134264261942642620CT24GENIChomozygous639255505
134264270642642707AG24GENIChomozygous639255506
134264282342642824CT15GENIChomozygous639255507
134264288542642886TG21GENIChomozygous639255508
134264322042643228GAAGGAAG--------8GENIChomozygous750559716
134264406342644064TC18GENICpossibly homozygous639255509
134264535442645355CCCA18GENICheterozygous750559718
134264536242645468ACACACATACCACAAGCACACACACACACACACACATACCACATGAACACATACACACACACACTCAAATACACATACACACATGTACTCACACACATGCATACAT----------------------------------------------------------------------------------------------------------40GENICheterozygous750559719
134264660242646603TTGATA8GENIChomozygous750559720
134264829142648292AAACACACACACAC14GENIChomozygous750559721
134264830742648308GC19GENIChomozygous639255510
134264869142648692AAGT14GENICpossibly homozygous750559724
134264910742649109CG--13GENICheterozygous750559725