chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105869097758690978CT24GENIChomozygous626111727
105869150058691501GA24GENIChomozygous626111728
105869150958691510AG22GENIChomozygous626111729
105869207058692071TC16GENIChomozygous626111730
105869229758692303TTTTTT------3GENICheterozygous743064112
105869230158692303TT--3GENICheterozygous743064113
105869272158692722GT23GENICpossibly homozygous626111731
105869286058692861GA26GENIChomozygous626111732
105869332458693325CT34GENIChomozygous626111733
105869344758693448AG23GENIChomozygous626111734
105869353558693540ACAAA-----24GENIChomozygous743064114
105869392358693924GA40GENIChomozygous626111735
105869392758693935ACACACAT--------45GENIChomozygous743064115
105869556558695566TA27GENIChomozygous626111736
105869583258695833AG30GENIChomozygous626111737
105869600158696002CCAA31GENIChomozygous743064116
105869710758697108AG13GENIChomozygous626111738
105869722958697230GT17GENIChomozygous626111739
105869830558698306TA27GENIChomozygous626111740
105869856958698573GGTA----21GENIChomozygous743064117
105869861258698613CT32GENIChomozygous626111741
105869889858698899TC29GENIChomozygous626111742
105869904858699049TTA14GENICheterozygous743064118
105869904858699049TTAA14GENICpossibly homozygous743064119
105870017358700174GA22GENIChomozygous626111743
105870048458700485CT24GENIChomozygous626111744
105870066258700663TG25GENIChomozygous626111745
105870081758700818GA17GENIChomozygous626111746
105870087258700873GA20GENIChomozygous626111747
105870137458701375GA32GENIChomozygous626111748
105870155258701553GA27GENIChomozygous626111749
105870406558704066GA17GENIChomozygous626111750
105870428358704284AAACACACACAC5GENIChomozygous743064123
105870670758706708AG16GENIChomozygous626111751
105870704858707049AG19GENIChomozygous626111752
105870828758708288CT19GENIChomozygous626111753
105870870458708705GA23GENIChomozygous626111754
105870924058709241AT32GENIChomozygous626111755
105870987558709876CT27GENIChomozygous626111756