chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148109121148109122TG23GENIChomozygous111768619
3148109320148109321TC19GENIChomozygous111768621
3148109322148109323TC19GENIChomozygous111768623
3148110320148110321GA11GENIChomozygous111768625
3148110526148110527TA26GENIChomozygous111768627
3148110853148110854GA28GENIChomozygous119652193
3148110854148110855AT31GENIChomozygous111768629
3148111105148111106TC21GENIChomozygous111768631
3148111729148111730AG32GENIChomozygous111768633
3148111922148111923TC20GENIChomozygous111768635
3148112001148112002AG15GENIChomozygous111768637
3148112438148112439TC25GENIChomozygous111768639
3148112743148112744TC21GENIChomozygous111768641
3148112913148112914GA21GENIChomozygous111768643
3148113407148113408CT13GENIChomozygous111768645
3148113582148113583AG13GENIChomozygous111768647
3148113945148113946CT15GENIChomozygous111768649
3148114160148114161CT21GENIChomozygous111768651
3148114496148114497GC24GENICpossibly homozygous111768655
3148114830148114831AG19GENIChomozygous111768657
3148114903148114904TC23GENIChomozygous111768659
3148115626148115627TC27GENIChomozygous111768661
3148115832148115833CT32GENIChomozygous111768663
3148116979148116980AG7GENIChomozygous111768665