chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228661637228661638TC43GENIChomozygous61107344
1228661888228661889GC56GENIChomozygous61107345
1228662170228662171GA74GENIChomozygous61107346
1228662393228662394CT68GENIChomozygous61107347
1228662746228662747CCGT20GENICpossibly homozygous61107348
1228664212228664213GA43GENIChomozygous61107349
1228665193228665194TC27GENICpossibly homozygous61107350
1228666155228666156AG43GENIChomozygous61107351
1228669606228669607GA53GENIChomozygous61107352
1228669631228669632TC44GENIChomozygous61107353
1228670146228670147AG40GENIChomozygous61107354
1228671386228671387GA65GENIChomozygous61107355
1228673220228673224AAAC----32GENIChomozygous61107356
1228673616228673617CT65GENIChomozygous61107357
1228675201228675202TC67GENIChomozygous61107358
1228675312228675313CT56GENIChomozygous61107359
1228675817228675819CA--23GENIChomozygous61107360
1228675822228675825GCC---22GENIChomozygous61107361
1228676534228676535GT35GENICpossibly homozygous61107362
1228676585228676586CCT15GENICheterozygous61107363
1228676585228676586CCTT15GENICheterozygous61107364
1228678058228678059GA54GENIChomozygous61107365
1228678104228678105AG68GENIChomozygous61107366
1228678862228678863CA46GENIChomozygous61107367
1228678931228678932AG41GENICpossibly homozygous61107368
1228680073228680074CT59GENIChomozygous61107369
1228681222228681223AT44GENIChomozygous61107370