chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109294823092948231TC12GENIChomozygous804109227
109294897692948977TC15GENIChomozygous804109228
109294929592949296CT12GENIChomozygous804109229
109294937292949373AT13GENIChomozygous804109230
109294939092949391TC13GENIChomozygous804109231
109294957992949580AG24GENIChomozygous804109232
109294977492949775CT24GENIChomozygous804109233
109294992192949922CT25GENIChomozygous804109234
109294996492949965CA27GENICpossibly homozygous804109235
109295023892950239CT17GENIChomozygous804109236
109295046692950467CT7GENIChomozygous804109237
109295047892950479TC8GENIChomozygous804109238
109295048292950483GT8GENIChomozygous804109239
109295049392950494CT8GENIChomozygous804109240
109295080492950805GA18GENIChomozygous804109241
109295087392950874CT20GENIChomozygous804109242
109295100592951006AC16GENIChomozygous804109243
109295107892951079GA11GENIChomozygous804109244
109295117092951171CA13GENIChomozygous804109245
109295119692951197GT11GENIChomozygous804109246
109295126592951266TA14GENIChomozygous804109247
109295127892951279CT19GENIChomozygous804109248
109295141992951420GA13GENIChomozygous804109249
109295160992951610CT8GENIChomozygous804109250
109295179092951791GT27GENIChomozygous804109251
109295182692951827GT16GENIChomozygous804109252
109295252492952525CT2GENIChomozygous804109253
109295259992952600CT4GENIChomozygous804109254
109295260292952603GA4GENIChomozygous804109255
109295260992952610GA4GENIChomozygous804109256
109295335992953360GA24GENIChomozygous804109257
109295363092953631GC25GENIChomozygous804109258
109295366292953663GA24GENIChomozygous804109259
109295469192954692AG9GENIChomozygous804109260
109295620092956201GA14GENICpossibly homozygous804109261
109295805792958058AG15GENIChomozygous804109262