chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25721721657217217AG10GENIChomozygous60211766
25721819257218193AG10GENICheterozygous60211767
25721823557218236GT7GENIChomozygous60211768
25722003557220036GT9GENIChomozygous60211769
25722023257220233CT5GENIChomozygous60211770
25722167357221674GA14GENIChomozygous60211771
25722267657222677G-7GENICpossibly homozygous60211772
25722343257223433AG12GENIChomozygous60211773
25722458957224590GGA12GENIChomozygous60211774
25722817657228177A-10GENIChomozygous60211776
25722827157228272TA13GENIChomozygous60211777
25723009657230097AG18GENIChomozygous60211778
25723051057230511TC22GENICpossibly homozygous60211779
25723292557232927TT--9GENIChomozygous60211780
25723294757232952TTTTG-----4GENICheterozygous60211781
25723361257233613TTATA3GENIChomozygous58833656
25723369257233693TA17GENICpossibly homozygous60211784
25723426057234261C-3GENICheterozygous60480736
25723426557234266C-3GENICheterozygous60480737
25723518357235184CCA1GENIChomozygous60566926
25723532657235327C-9GENIChomozygous60211786
25723634957236350T-15GENICheterozygous60211787
25723648157236482AG9GENIChomozygous60211788
25723865657238657AG8GENICpossibly homozygous60211789
25723902657239027GGT1GENIChomozygous58833657