chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122709649427096495GGAGCCT16GENIChomozygous50152159
122709732027097321TTTTTTTTTTTG3GENIChomozygous50539532
122709787927097880TC12GENIChomozygous50152177
122709790427097905CCT10GENICheterozygous50569646
122709790727097910TTT---10GENICheterozygous50562401
122709919227099193GA18GENIChomozygous50152185
122709922727099228AG16GENIChomozygous50152187
122709930527099314GGGGGGGGG---------1GENIChomozygous50152195
122709931327099314GGTT1GENIChomozygous50597962
122709951327099514TA8GENICheterozygous50301311
122709993327099939GTGTGT------5GENICheterozygous50539534
122709993527099939GTGT----5GENICheterozygous50604232
122710031927100320CCTTTTT11GENICheterozygous50152199
122710167227101673T-17GENIChomozygous50152209
122710255627102557TC19GENIChomozygous50152221
122710302627103027GC28GENIChomozygous50152225
122710315027103151TC28GENIChomozygous50152227
122710361727103619GG--8GENIChomozygous50152229
122710031927100320CCT11GENICheterozygous50374168
122710178227101783GA35GENIChomozygous50374170
122710367627103677CCT14GENIChomozygous50374172
122710383027103834ATAG----31GENIChomozygous50374176
122710473027104731GA41GENIChomozygous50374178
122710504427105045TA15GENIChomozygous50374180
122710504627105047AC15GENIChomozygous50374182
122710592127105922TC39GENIChomozygous50152244
122710628827106289GA16GENIChomozygous50374184
122710638827106389TA26GENIChomozygous50152250
122710676727106768GA23GENIChomozygous50374186
122710703227107033TTAAAG23GENIChomozygous50152256
122710801027108011AG15GENIChomozygous50152270
122710706227107063GA25GENIChomozygous50152260
122710707027107071TTGTGG23GENIChomozygous50152262
122710707527107076AG28GENIChomozygous50374188
122710812127108124TCT---5GENIChomozygous50539535
122710817727108178GA9GENIChomozygous50152274
122710833227108333AC37GENIChomozygous50374190
122710920527109206A-29GENIChomozygous50374192