chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706760647067607GA25GENIChomozygous964658036
104706797347067974AC35GENIChomozygous964658037
104706890447068905CT18GENIChomozygous964658038
104706893147068932CA16GENIChomozygous964658039
104708237347082374GA28GENIChomozygous964658040
104708241747082418AC28GENIChomozygous964658041
104708255747082558GA33GENIChomozygous964658042
104708308147083082GA31GENIChomozygous964658043
104708432247084323AG16GENIChomozygous964658044
104708446147084462TC28GENIChomozygous964658045
104708587347085874TC46GENIChomozygous964658046
104708642247086423GC34GENIChomozygous964658047
104708650047086501AG28GENIChomozygous964658048
104708665247086653CA20GENIChomozygous964658049
104708819347088194GT41GENIChomozygous964658050
104708985847089859GA28GENIChomozygous964658051
104709009547090096TA12GENIChomozygous964658052
104709048247090483TC35GENIChomozygous964658053
104709050647090507GT39GENIChomozygous964658054
104709079447090795CA39GENIChomozygous964658055
104709128847091289GT31GENIChomozygous964658056
104709153347091534CT47GENIChomozygous964658057
104709154247091543CT43GENIChomozygous964658058
104709189647091897CT36GENIChomozygous964658059
104709296347092964TC31GENIChomozygous964658060
104709340447093405TC29GENIChomozygous964658061
104709370847093709TC21GENIChomozygous964658062
104709401947094020TC12GENIChomozygous964658063
104709540047095401AC18GENIChomozygous964658064
104709700447097005TC29GENIChomozygous964658065
104710045347100454CT15GENIChomozygous964658066
104710175847101759CT40GENIChomozygous964658067
104710532847105329TC40GENIChomozygous964658068
104710603047106031TC17GENIChomozygous964658069
104710799847107999AG33GENIChomozygous964658070
104710810447108105CG29GENIChomozygous964658071