chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25721721657217217AG7GENIChomozygous60211766
25721819257218193AG8GENIChomozygous60211767
25721823557218236GT15GENIChomozygous60211768
25722003557220036GT19GENICpossibly homozygous60211769
25722023257220233CT6GENIChomozygous60211770
25722167357221674GA16GENIChomozygous60211771
25722267657222677G-11GENICheterozygous60211772
25722343257223433AG18GENIChomozygous60211773
25722458957224590GGA11GENIChomozygous60211774
25722817657228177A-8GENIChomozygous60211776
25722827157228272TA10GENIChomozygous60211777
25723009657230097AG21GENIChomozygous60211778
25723051057230511TC10GENIChomozygous60211779
25723292557232927TT--5GENIChomozygous60211780
25723295957232963TTGG----4GENICheterozygous61460709
25723361257233613TTATA11GENICpossibly homozygous58833656
25723369257233693TA17GENICheterozygous60211784
25723532657235327C-11GENIChomozygous60211786
25723634957236350T-17GENICpossibly homozygous60211787
25723648157236482AG5GENIChomozygous60211788
25723865657238657AG6GENIChomozygous60211789
25723902657239027GGT2GENICheterozygous58833657