chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221069198221069199CT16GENIChomozygous62589419
1221069421221069422TC24GENIChomozygous61093617
1221069528221069529GA21GENIChomozygous61093618
1221072582221072583AG12GENIChomozygous61595658
1221074274221074275GT28GENIChomozygous61093620
1221074279221074280CT28GENIChomozygous62589420
1221074705221074706AG14GENIChomozygous62589421
1221077962221077982ACACACACACACACACACAC--------------------6GENIChomozygous62556258
1221078775221078776TTCC12GENIChomozygous61595663
1221078776221078777AAGGTC12GENIChomozygous61595665
1221079359221079360CCT11GENICpossibly homozygous61093625
1221079896221079897T-4GENIChomozygous62236975
1221080275221080276AC19GENIChomozygous61093628