chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103553958335539584GT8GENIChomozygous116867245
103554148835541489AT14GENIChomozygous116558078
103554172835541729GT27GENIChomozygous116558080
103554191835541919GA28GENIChomozygous116558082
103554228335542284CA28GENIChomozygous116558084
103554272835542729AG21GENIChomozygous116558086
103554286035542861TC28GENIChomozygous116558088
103554308835543089TC17GENIChomozygous116558090
103554454235544543GA22GENIChomozygous116558092
103554610035546101TC26GENIChomozygous116558094
103554647035546471CT28GENICpossibly homozygous116558096
103554771935547720TA22GENIChomozygous116867247
103554950035549501CT47GENIChomozygous116558098
103555070135550702GA17GENIChomozygous116558100
103555231935552320CT14GENIChomozygous116558102
103556100635561007CT23GENIChomozygous116558110
103556800935568010CA12GENIChomozygous116867249
103556874635568747CA18GENIChomozygous116558114
103558370435583705AG16GENIChomozygous116757874
103559489135594892CT31GENIChomozygous116558120
103559615835596159GC24GENIChomozygous116558122
103559664135596642CT22GENIChomozygous116558124
103559681135596812TG20GENIChomozygous116558126
103559681235596813GT20GENIChomozygous116558128
103559681635596817CT21GENIChomozygous116558130
103559685335596854AG20GENIChomozygous116558132
103559690235596903CT29GENIChomozygous116558136
103559796035597961AG16GENIChomozygous116558138
103559813535598136AG22GENIChomozygous116558140
103559848135598482TC24GENIChomozygous116558142
103559987535599876CT21GENIChomozygous116558144
103560158035601581CT21GENIChomozygous116558146
103560465835604659AG26GENIChomozygous116558148
103560770535607706GA30GENIChomozygous116558152