chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64051100940511011GT--15GENICpossibly homozygous54869577
64051101140511012GA16GENICpossibly homozygous56197422
64051159940511600AG27GENIChomozygous54869578
64051222540512226GA17GENIChomozygous54869579
64051275140512752CT23GENIChomozygous54869580
64051279640512797TC21GENIChomozygous54869581
64051298240512983GT21GENIChomozygous54869582
64051377440513775TC20GENIChomozygous54869583
64051395640513957AG24GENIChomozygous54869584
64051396240513963CT25GENIChomozygous54869585
64051414040514141TC20GENIChomozygous54869586
64051421140514212TC20GENIChomozygous54869587
64051521040515211CG12GENIChomozygous54869588
64051524540515246GGTT13GENIChomozygous54869589
64051541140515412TC25GENIChomozygous54869590
64051542340515424AG30GENIChomozygous54869591
64051663240516634GT--10GENICpossibly homozygous54362298
64052032540520326CT24GENIChomozygous54869592
64052059740520598TC26GENIChomozygous54869593
64052120340521204TC22GENIChomozygous54869594
64052289040522891GT22GENIChomozygous54869595
64052402140524022CT24GENIChomozygous54869596
64052426540524266TTCACCACCACCACCACCACCACCACCAC5GENIChomozygous56197423
64052443040524431AC17GENIChomozygous54869599
64052470940524710GT25GENIChomozygous54869600
64052522340525224AG20GENIChomozygous54869601
64052529640525297GA26GENIChomozygous54869602
64052535140525352CT20GENIChomozygous54869603
64052543640525437AC26GENIChomozygous54869604
64052587940525880CT20GENIChomozygous54869605