chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655562756555628AG32GENIChomozygous789550109
55655610056556101TG22GENIChomozygous789550110
55655739456557395TC21GENIChomozygous789550111
55655772456557725CT21GENIChomozygous789550112
55655807256558073GA36GENIChomozygous789550113
55655837556558376TC26GENIChomozygous789550114
55655883856558839AT27GENIChomozygous789550115
55655962256559623GC22GENIChomozygous789550116
55655994156559942AC10GENIChomozygous789550117
55656006956560070GA12GENIChomozygous789550118
55656018256560183CT55GENICheterozygous789550119
55656053356560534CT22GENICheterozygous789550120
55656055656560557CT29GENICheterozygous789550121
55656059356560594TC58GENICheterozygous789550122
55656069356560694TC36GENICheterozygous789550123
55656073656560737CT63GENICheterozygous789550124
55656074356560744CT63GENICheterozygous789550125
55656080256560803CT47GENICheterozygous789550126
55656081356560814AG44GENICheterozygous789550127
55656093156560932CT32GENICheterozygous789550128
55656100456561005AG27GENIChomozygous789550129
55656114056561141GT20GENIChomozygous789550130
55656152156561522AT30GENIChomozygous789550131
55656160756561608AT30GENIChomozygous789550132
55656190156561902AT25GENICpossibly homozygous789550133
55656318756563188TC30GENIChomozygous789550134
55656521156565212AG34GENIChomozygous789550135
55656558756565588AC32GENICheterozygous789550136
55656567156565672CA27GENIChomozygous789550137
55656583756565838CT24GENIChomozygous789550138
55656616956566170TC29GENIChomozygous789550139