chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
725049012504902TA22GENIChomozygous53765669
725049882504989CCTTTTTTTTTT10GENICheterozygous54951282
725057562505757AG36GENIChomozygous53765671
725064812506482A-14GENIChomozygous53765673
725065172506518CT18GENIChomozygous53765674
725066872506688GA30GENIChomozygous53765675
725067092506713GTGT----28GENIChomozygous53765676
725069272506928TTGACACACACACACA5GENIChomozygous54951288
725072402507241GGA31GENICpossibly homozygous53765679
725073102507311GGTT21GENIChomozygous53765680
725093382509339AC14GENIChomozygous53765683
725100642510065TG8GENIChomozygous53765684
725103722510373AG16GENIChomozygous53765685
725114682511471TTT---23GENICpossibly homozygous53765686
725114692511471TT--23GENICheterozygous53765687
725114872511488GT24GENIChomozygous53765688
725116162511617TC28GENIChomozygous53765690
725116352511636CCA23GENICpossibly homozygous53765691
725116372511638A-23GENICheterozygous54951290