chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106048787760487878AT15GENIChomozygous632248585
106048787860487879AC15GENICpossibly homozygous632248586
106048794960487950TG27GENIChomozygous632248587
106048799260487993AG29GENIChomozygous632248588
106048799760487998CA26GENIChomozygous632248589
106048802560488026AT22GENIChomozygous632248590
106048806360488064TA22GENIChomozygous632248591
106048822360488224CT28GENIChomozygous632248592
106048832760488328AG33GENIChomozygous632248593
106048834960488350CT37GENIChomozygous632248594
106048835660488357TC36GENIChomozygous632248595
106048838660488387AT41GENIChomozygous632248596
106048844960488450GA41GENIChomozygous632248597
106048845060488451GA42GENIChomozygous632248598
106048846260488463TC40GENIChomozygous632248599
106048861060488611AG34GENIChomozygous632248600