chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47092129570921296CT20GENIChomozygous119512054
47092552070925521GA23GENIChomozygous113032997
47092569370925694GT26GENICpossibly homozygous119512056
47092619270926193CT11GENIChomozygous112703738
47092757470927575GA26GENIChomozygous112703744
47092772670927727CT22GENIChomozygous112703746
47092886170928862TC32GENIChomozygous112703750
47092903270929033CA29GENIChomozygous112703752
47093026670930267AT25GENIChomozygous119512058
47093280470932805TC15GENIChomozygous113033000
47093353370933534TC20GENIChomozygous113033001
47093356870933569GA21GENIChomozygous113033002
47093360770933608AG19GENIChomozygous113033003
47093363470933635GA18GENIChomozygous113033004
47093383070933831TC13GENIChomozygous113033005
47093410470934105AG13GENIChomozygous113033006