chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1238500223850024CT--3GENICheterozygous50526070
1238524233852424CCTGTG13GENICpossibly homozygous50001308
1238571313857141CACACACACA----------17GENICheterozygous50001313
1238571373857141CACA----17GENICpossibly homozygous50559688
1238658933865894T-200GENICheterozygous50001327
1238661473866149CT--102GENICpossibly homozygous50001331
1238661573866159CT--60GENICheterozygous50001332
1238661763866181GCTCT-----23GENICheterozygous50526080
1238661843866191GAGCTCT-------12GENICheterozygous50567060
1238662783866279CCAGCAGG4GENIChomozygous50567061
1238663713866372AAACCAAACCAC75GENICheterozygous50526087
1238715533871554C-1GENIChomozygous50001353
1238835503883552AC--15GENICheterozygous50567062
1238884383888439AT22GENICheterozygous50274344
1238987223898723A-6GENICheterozygous50567063
1238994983899502TGGA----4GENIChomozygous50567064
1239074693907470TTG13GENICheterozygous50567065
1239098073909808GGA9GENIChomozygous50001487
1239227023922704GA--14GENIChomozygous50567066
1239249673924969CA--21GENICheterozygous50001521
1239250923925099CACACAC-------9GENICheterozygous50526154
1239251013925106CACAC-----12GENICheterozygous50526156
1239254493925451GA--9GENIChomozygous50567067
1239270453927046CCCA17GENICheterozygous50567068
1239317063931712ATATAG------2GENIChomozygous50567069
1239504263950430CTCT----7GENICheterozygous50567070
1239504283950430CT--7GENICheterozygous50526176
1239617703961772TC--17GENICheterozygous50526180
1239639673963968GGT10GENICheterozygous50567071
1239639683963969T-10GENICheterozygous50393968
1239653663965367GGGATA13GENIChomozygous50567072
1239654743965475TTGATA13GENIChomozygous50001610
1239669143966916AC--8GENICheterozygous50567073
1239696483969652TTAT----2GENIChomozygous50567074
1239719543971958AGAG----8GENICheterozygous50567075
1239822963982300ATAG----14GENIChomozygous50567076
1239872333987234AAAC12GENICheterozygous50357685
1239875453987546GGT8GENICheterozygous50567077
1239875673987568GT12GENIChomozygous50503159