chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101656656216566563CA24GENIChomozygous532348742
101656660616566607GA25GENIChomozygous532348743
101656664216566643AG24GENIChomozygous532348744
101656689916566900AG25GENIChomozygous532348745
101656706416567065CT19GENIChomozygous532348746
101656720016567201TC26GENIChomozygous532348747
101656756216567563GA10GENIChomozygous532348748
101656761616567617T-16GENIChomozygous694364763
101656780116567802AG20GENIChomozygous532348749
101656811216568113TC44GENICpossibly homozygous532348750
101656820616568207TTA21GENICpossibly homozygous694364764
101656828316568284CG23GENIChomozygous532348751
101656831216568313TTA17GENIChomozygous694364765
101656857116568572TC22GENIChomozygous532348752
101656861516568616CT26GENIChomozygous532348753
101656900616569007CG29GENIChomozygous532348754
101656932216569323CG21GENIChomozygous532348755
101656934916569350CG17GENIChomozygous532348756
101656937816569379TC18GENIChomozygous532348757
101657047516570476CT20GENIChomozygous532348758
101657109116571092GA24GENIChomozygous532348759
101657138116571382CT28GENIChomozygous532348760
101657157116571572CG22GENIChomozygous532348761
101657302916573030CT27GENICheterozygous532348762
101657357416573575AT34GENIChomozygous532348763
101657421616574217GT32GENIChomozygous532348764
101657444816574449CT28GENIChomozygous532348765
101657475516574756GA19GENIChomozygous532348766
101657514416575145TC28GENICpossibly homozygous532348767
101657561316575614AC38GENIChomozygous529678404
101657587316575874AG15GENICheterozygous529678405
101657591016575911CT17GENIChomozygous529678406
101657597316575974GGC17GENIChomozygous694364766
101657653716576538GGT9GENICpossibly homozygous694364767