chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35999601159996012TA22GENIChomozygous111584587
35999856259998563GT23GENIChomozygous111584588
36000057360000574CA29GENIChomozygous111584589
36000107060001071GA16GENIChomozygous111584590
36000226860002269CT33GENIChomozygous111584591
36000245360002454AG23GENIChomozygous111584592
36000305160003052CT33GENIChomozygous111584593
36000487560004876CT20GENIChomozygous111584594
36000733260007333CT16GENIChomozygous111584595
36000752660007527CA21GENIChomozygous111584596
36001006660010067CG34GENIChomozygous111584597
36001068060010681GC34GENIChomozygous111584598
36001458260014583AG20GENIChomozygous111584600
36001697660016977GC24GENIChomozygous111584601
36001779460017795GA17GENIChomozygous111584602
36001864660018647CG22GENIChomozygous111584603
36001866860018669AG21GENIChomozygous111584604
36001912060019121AG20GENIChomozygous111584605
36001918660019187GA18GENIChomozygous111584606
36001949060019491AG32GENIChomozygous111584607
36001952860019529CT30GENIChomozygous111584608
36001966760019668GA23GENIChomozygous111584609
36001972660019727CT17GENIChomozygous111584610
36001974360019744CT18GENIChomozygous111584611
36002010060020101AG27GENIChomozygous111584612
36002143660021437CT35GENIChomozygous111584613
36002154560021546GT20GENIChomozygous111584614
36002187860021879AG33GENIChomozygous111584615
36002210660022107GA12GENIChomozygous111584616
36002353260023533GA30GENIChomozygous111584624