chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71199359911993600GT49GENICpossibly homozygous115569358
71199446211994463TC41GENIChomozygous115569359
71199654211996543GA63GENIChomozygous115569360
71199687111996872TC50GENIChomozygous115569361
71199716711997168TC49GENIChomozygous115569362
71199730511997306TC32GENIChomozygous115569363
71199751311997514CT50GENIChomozygous115569364
71199971411999715CT29GENIChomozygous115569365
71200046212000463TC51GENIChomozygous115569366
71200054112000542CT46GENIChomozygous115569367