chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105869097758690978CT14GENIChomozygous646185138
105869150058691501GA11GENIChomozygous646185139
105869150958691510AG11GENIChomozygous646185140
105869207058692071TC23GENIChomozygous646185141
105869272158692722GT14GENIChomozygous646185142
105869286058692861GA18GENIChomozygous646185143
105869332458693325CT23GENIChomozygous646185144
105869344758693448AG24GENIChomozygous646185145
105869353558693540ACAAA-----22GENIChomozygous754821960
105869392358693924GA24GENIChomozygous646185146
105869392758693935ACACACAT--------26GENIChomozygous754821961
105869556558695566TA23GENIChomozygous646185147
105869583258695833AG20GENIChomozygous646185148
105869600158696002CCAA23GENIChomozygous754821962
105869710758697108AG15GENIChomozygous646185149
105869722958697230GT15GENIChomozygous646185150
105869830558698306TA17GENIChomozygous646185151
105869856958698573GGTA----16GENIChomozygous754821963
105869861258698613CT22GENIChomozygous646185152
105869889858698899TC23GENIChomozygous646185153
105869904858699049TTA21GENICheterozygous754821964
105869904858699049TTAA21GENICpossibly homozygous754821965
105870017358700174GA15GENIChomozygous646185154
105870048458700485CT7GENIChomozygous646185155
105870066258700663TG22GENIChomozygous646185156
105870081758700818GA17GENIChomozygous646185157
105870087258700873GA18GENIChomozygous646185158
105870137458701375GA12GENIChomozygous646185159
105870155258701553GA17GENIChomozygous646185160
105870406558704066GA11GENICheterozygous646185161
105870428358704284AAACACACACAC3GENIChomozygous754821969
105870670758706708AG18GENIChomozygous646185162
105870704858707049AG14GENIChomozygous646185163
105870828758708288CT23GENIChomozygous646185164
105870870458708705GA13GENIChomozygous646185165
105870924058709241AT25GENIChomozygous646185166
105870987558709876CT14GENIChomozygous646185167