chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228661637228661638TC30GENIChomozygous638805295
1228661888228661889GC23GENIChomozygous638805296
1228662170228662171GA22GENIChomozygous638805297
1228662393228662394CT23GENIChomozygous638805298
1228662746228662747CCGT23GENICheterozygous750260639
1228662746228662747CCGTGTGTGT23GENICheterozygous750260640
1228664212228664213GA23GENIChomozygous638805299
1228665193228665194TC18GENIChomozygous638805300
1228666155228666156AG27GENICpossibly homozygous638805301
1228669606228669607GA38GENIChomozygous638805302
1228669631228669632TC44GENIChomozygous638805303
1228670146228670147AG32GENIChomozygous638805304
1228671386228671387GA44GENIChomozygous638805305
1228673220228673224AAAC----21GENIChomozygous750260641
1228673616228673617CT30GENIChomozygous638805306
1228674328228674340GTGTGTGTGTGT------------9GENICpossibly homozygous750260643
1228675201228675202TC23GENIChomozygous638805307
1228675312228675313CT17GENIChomozygous638805308
1228675817228675819CA--20GENIChomozygous750260645
1228675822228675825GCC---23GENIChomozygous750260646
1228676534228676535GT18GENIChomozygous638805309
1228676585228676586CCTT13GENICheterozygous750260647
1228676585228676586CCT13GENICheterozygous750260648
1228678058228678059GA29GENIChomozygous638805310
1228678104228678105AG23GENIChomozygous638805311
1228678862228678863CA22GENIChomozygous638805312
1228678931228678932AG20GENIChomozygous638805313
1228680073228680074CT20GENIChomozygous638805314
1228681222228681223AT14GENIChomozygous638805315