chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122709649427096495GGAGCCT23GENIChomozygous50152159
122709732527097326G-21GENICheterozygous50152167
122709787927097880TC27GENIChomozygous50152177
122709790627097908TT--5GENICheterozygous50374166
122709816227098163TG34GENICheterozygous50152181
122709919227099193GA42GENIChomozygous50152185
122709922727099228AG32GENIChomozygous50152187
122709929527099314TTTTTTTTTTGGGGGGGGG-------------------13GENICheterozygous50152191
122709929727099314TTTTTTTTGGGGGGGGG-----------------16GENICheterozygous50152193
122709930527099314GGGGGGGGG---------10GENIChomozygous50152195
122710031927100320CCTTTTT34GENICheterozygous50152199
122710031927100320CCT34GENICpossibly homozygous50374168
122710167227101673T-22GENIChomozygous50152209
122710178227101783GA45GENIChomozygous50374170
122710255627102557TC48GENIChomozygous50152221
122710302627103027GC63GENIChomozygous50152225
122710315027103151TC37GENICpossibly homozygous50152227
122710361727103619GG--6GENIChomozygous50152229
122710367627103677CCT26GENIChomozygous50374172
122710367927103680TTA15GENICheterozygous50374174
122710383027103834ATAG----29GENIChomozygous50374176
122710473027104731GA60GENIChomozygous50374178
122710504427105045TA45GENICpossibly homozygous50374180
122710504627105047AC44GENICpossibly homozygous50374182
122710592127105922TC59GENIChomozygous50152244
122710628827106289GA54GENICpossibly homozygous50374184
122710638827106389TA53GENIChomozygous50152250
122710676727106768GA48GENIChomozygous50374186
122710703227107033TTAAAG34GENIChomozygous50152256
122710706227107063GA41GENIChomozygous50152260
122710707027107071TTGTGG31GENIChomozygous50152262
122710707527107076AG38GENIChomozygous50374188
122710801027108011AG52GENICpossibly homozygous50152270
122710817727108178GA17GENICpossibly homozygous50152274
122710833227108333AC26GENIChomozygous50374190
122710920527109206A-38GENIChomozygous50374192