chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
188642187986421880CG37GENICheterozygous791843647
188642191786421918CT35GENICheterozygous791843648
188642192586421926TC38GENICheterozygous791843649
188645293286452933AT16GENIChomozygous791843650
188647029986470300AC7GENIChomozygous791843651
188647043286470433GT12GENIChomozygous791843652
188647060286470603AG13GENIChomozygous791843653
188647829086478291AG8GENICpossibly homozygous791843654
188662696386626964GA16GENICheterozygous791843655
188663630386636304AG8GENIChomozygous791843656
188668228286682283GT6GENICheterozygous791843657
188672285986722860CT9GENIChomozygous791843658
188672860886728609AC14GENIChomozygous791843659
188678361586783616AG14GENICheterozygous791843660
188679598686795987GT3GENIChomozygous791843661
188680969186809692CT9GENIChomozygous791843662
188681140186811402AG14GENICheterozygous791843663
188681140986811410GA14GENICheterozygous791843664
188683897986838980TG29GENIChomozygous791843665
188684603486846035CG17GENIChomozygous791843666
188684605486846055CG20GENIChomozygous791843667
188685882586858826AG17GENICheterozygous791843668
188685882786858828CT16GENICheterozygous791843669
188685885286858853TG17GENICheterozygous791843670
188685889286858893AG22GENICheterozygous791843671