chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137880662178806622GGA1GENIChomozygous50552629
137880704578807046GGA1GENIChomozygous50435930
137880789078807891TC23GENIChomozygous49829915
137880880678808807CT27GENIChomozygous49829932
137880890678808907AAGTAC27GENIChomozygous49829934
137880928778809288AG27GENIChomozygous49829938
137880958078809581CT26GENIChomozygous49829940
137881040778810408CT5GENIChomozygous50435932
137881056978810570AG17GENIChomozygous49829960
137881064678810647GC20GENIChomozygous49829964
137881123678811237AT21GENIChomozygous49829977
137881230378812307ACAC----20GENIChomozygous49829996
137881240678812407CT28GENIChomozygous50435934
137881277878812779GA19GENIChomozygous50435936
137881347578813476TTA2GENIChomozygous49830011
137881404378814044GA17GENIChomozygous50435938
137881467078814671AG24GENIChomozygous49830028
137881512678815127TA14GENIChomozygous49830033
137881550778815508TTA14GENIChomozygous50435944
137881680878816809TC23GENIChomozygous50435946
137881701078817016ACGCTG------19GENIChomozygous49830060
137881710278817103TC23GENIChomozygous50435950
137881710578817106AG24GENIChomozygous50435952
137881729678817297TC27GENIChomozygous49830061
137881822778818228CT16GENIChomozygous50435955
137881837078818371AG22GENIChomozygous50435957
137881879078818791TC10GENIChomozygous50435959
137882004178820042CT24GENIChomozygous50435961
137882022478820225TA18GENIChomozygous49830098
137881981878819819TTAC5GENICheterozygous50524377
137881337178813372TTAGACAAGATGGATGAAGCAAAGAAGTGCAGACC5GENIChomozygous50524375