chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121811548018115481CT18GENICpossibly homozygous598053538
121811593818115939TTA7GENICheterozygous726493511
121811672718116728AG10GENICpossibly homozygous597139810
121811737618117377AG7GENIChomozygous597139811
121811745318117454TC4GENIChomozygous598053539
121811792618117927TA1GENIChomozygous597139812
121811836018118361GA13GENIChomozygous598053540
121811839518118396AAC8GENIChomozygous726493512
121811888318118884GA9GENIChomozygous597139813
121811899218118993TTC3GENICheterozygous726493513
121811929718119300GGG---10GENIChomozygous726493514
121812003018120031GA30GENICpossibly homozygous598053541
121812023418120235CT14GENICpossibly homozygous598053542
121812290118122902AG3GENIChomozygous597139814