chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108923627489236275CG21GENIChomozygous117152493
108923627689236277CA22GENIChomozygous117152494
108923632589236326AG21GENIChomozygous117227889
108923755589237556CT17GENICheterozygous118129889
108923800389238004TC40GENIChomozygous116819783
108923910289239103CA39GENICheterozygous117068442
108923912089239121AT23GENIChomozygous117068444
108923974589239746AT42GENIChomozygous116819791
108924001689240017TC28GENIChomozygous116819793
108924023089240231GA31GENIChomozygous116902256
108923821989238220GA33GENIChomozygous116902250
108923823089238231GC30GENIChomozygous116902252
108923920789239208AG25GENIChomozygous116902254
108924023389240234CT29GENIChomozygous116902258
108924089289240893AG24GENIChomozygous116902260
108924146489241465AC39GENIChomozygous116902262
108924160489241605TC37GENIChomozygous116819797
108924177589241776GA10GENIChomozygous116902264
108924182989241830GA19GENIChomozygous116902266
108924267789242678TG25GENIChomozygous117087255
108924333989243340GA45GENIChomozygous116902268
108924363189243632AG29GENICpossibly homozygous116819801
108924316689243167AG23GENIChomozygous118048845
108924319989243200AG26GENIChomozygous118048846