chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214919309214919310GT14GENIChomozygous109192052
1214920102214920103GC10GENIChomozygous109192054
1214921439214921440CT16GENIChomozygous109192058
1214921840214921841GA25GENIChomozygous108533204
1214922114214922115CT35GENIChomozygous108533206
1214922559214922560CG31GENIChomozygous108533207
1214923709214923710TC18GENIChomozygous108533209
1214924207214924208CT21GENIChomozygous108990657
1214924358214924359GT19GENIChomozygous108533210
1214924516214924517TC25GENIChomozygous108533211
1214925348214925349GT29GENIChomozygous108533212
1214925907214925908TA35GENIChomozygous120475838
1214925908214925909CT35GENIChomozygous120475839
1214925916214925917TC36GENIChomozygous108533213
1214925920214925921TC36GENIChomozygous108533214
1214926127214926128CT27GENIChomozygous108533215
1214926216214926217GA30GENIChomozygous108533216
1214926375214926376CT28GENIChomozygous108533217
1214926992214926993GA21GENIChomozygous108533218
1214927111214927112TG20GENIChomozygous108533219
1214928116214928117GA18GENIChomozygous108533220
1214928359214928360AG17GENIChomozygous108533221
1214928839214928840TC12GENIChomozygous108533222
1214929260214929261CA23GENIChomozygous108533223
1214930438214930439TC18GENIChomozygous108533224
1214930635214930636GA11GENIChomozygous108533225
1214931485214931486GA20GENIChomozygous108533226
1214931961214931962AT30GENIChomozygous108533227
1214934101214934102AG29GENIChomozygous108533228
1214934380214934381CT26GENIChomozygous108533229
1214934728214934729TC20GENIChomozygous108533230
1214935151214935152CT13GENIChomozygous108533232
1214937708214937709AG23GENIChomozygous108533233
1214939307214939308GC21GENIChomozygous108533234
1214939882214939883TG10GENIChomozygous108533235
1214939975214939976GA23GENIChomozygous108533236
1214940130214940131GA28GENIChomozygous108533237
1214940500214940501GA24GENIChomozygous108533238
1214940511214940512GA26GENIChomozygous108533239