chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141246857141246858CCCCCACCCAACTT13GENIChomozygous54158119
7141247044141247045AG22GENIChomozygous54158120
7141247083141247084AG24GENICheterozygous54158121
7141247083141247084AAAAAGG22GENIChomozygous54158122
7141247987141247988AG51GENIChomozygous54158124
7141248571141248572GA40GENIChomozygous54678436
7141248581141248582CT41GENIChomozygous54158125
7141248690141248691TTG36GENIChomozygous54678438
7141248775141248776AG26GENIChomozygous54678440
7141248795141248796TC21GENIChomozygous54678442
7141249098141249099AG27GENIChomozygous54158127
7141249220141249221CT30GENIChomozygous54158128
7141249303141249304GA34GENIChomozygous54678444
7141249583141249584TG31GENIChomozygous54158130
7141249771141249773TA--44GENIChomozygous54678446
7141250216141250217TC39GENIChomozygous54158131
7141250217141250218GA38GENIChomozygous54678448
7141250527141250528GA34GENICpossibly homozygous54678450
7141250866141250867CT33GENIChomozygous54678452