chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150685716150685717TC26GENIChomozygous941112630
5150687272150687273CT23GENIChomozygous941112631
5150690664150690665GA31GENIChomozygous941112632
5150690906150690907TC38GENIChomozygous941112633
5150691388150691389CT9GENIChomozygous941112634
5150691794150691795TC30GENIChomozygous941112635
5150692118150692119TA4GENIChomozygous941112636
5150692120150692121GC4GENIChomozygous941112637
5150692122150692123TC8GENIChomozygous941112638
5150692332150692333GA32GENIChomozygous941112639
5150692912150692913CT20GENIChomozygous941112640
5150694695150694696CT19GENIChomozygous941112641
5150695760150695761CT24GENIChomozygous941112642
5150696424150696425TC16GENIChomozygous941112643
5150696850150696851GA11GENIChomozygous941112644
5150698973150698974CT28GENIChomozygous941112645
5150699625150699626GA9GENIChomozygous941112646
5150701338150701339CT37GENIChomozygous941112647
5150701466150701467TC26GENIChomozygous941112648
5150703071150703072AC25GENIChomozygous941112649