chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181793716117937162AG29GENIChomozygous971247084
181793737717937378CG32GENIChomozygous971247085
181793755417937555AC30GENIChomozygous971247086
181793780617937807GA34GENIChomozygous971247087
181793805517938056AG29GENIChomozygous971247088
181793814417938145AG29GENIChomozygous971247089
181793815417938155CT30GENIChomozygous971247090