chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96489978564899786TG26GENIChomozygous117577700
96489980764899808GA24GENIChomozygous117577702
96490002864900029GC17GENIChomozygous117577704
96490019564900196CT27GENIChomozygous117577706
96490044764900448GT26GENIChomozygous117577708
96490118264901183GA27GENIChomozygous117577710
96490147864901479CT7GENIChomozygous117577712
96490202164902022TC17GENIChomozygous117577714
96490250964902510CT25GENIChomozygous117577718
96490259964902600TG26GENIChomozygous117577720
96490422764904228AG16GENIChomozygous117577722
96490464064904641GT15GENIChomozygous117577724
96490505964905060TC22GENIChomozygous117577726
96490592364905924TC25GENIChomozygous117577728
96490637664906377GA20GENIChomozygous117577730
96490652764906528CT20GENIChomozygous117577732
96490685964906860CT20GENIChomozygous117577734
96490702964907030CT13GENIChomozygous117577736
96490750364907504AG3GENICheterozygous126610455
96490961464909615AT22GENIChomozygous117577738
96491035964910360GA11GENIChomozygous117577742
96491290564912906AG27GENIChomozygous117577744
96491308064913081AG20GENIChomozygous117577746
96491528664915287AG23GENIChomozygous117577748
96491559364915594CT19GENIChomozygous117577750
96491663164916632AC19GENIChomozygous117577752
96491925064919251GA22GENIChomozygous117577756
96492097264920973GA12GENIChomozygous117577760
96492104064921041GA21GENIChomozygous117577762
96492156064921561AG12GENIChomozygous117364621
96492171764921718TC23GENIChomozygous117577764
96492178664921787AG9GENIChomozygous117577766
96492248964922490TC24GENIChomozygous117364627