chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115141042115141043AG39GENIChomozygous68281305
8115142504115142505GA21GENIChomozygous68281307
8115143004115143005GA48GENIChomozygous68281309
8115144171115144172GA31GENIChomozygous68281311
8115144596115144597AG35GENICpossibly homozygous68281313
8115144654115144655GC26GENICheterozygous68281315
8115144674115144675GC21GENICheterozygous68281317
8115144767115144768GA40GENIChomozygous68281319
8115144956115144957AG39GENIChomozygous68281321
8115145004115145005AG53GENIChomozygous68281323
8115145180115145181GA35GENIChomozygous68281325
8115145750115145751TC41GENIChomozygous68281327
8115146418115146419TC37GENICpossibly homozygous68281329
8115146408115146409TC36GENICheterozygous68639309