chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7655440655441TG4GENIChomozygous137986879
7657077657078AG19GENIChomozygous137986880
7661049661050CT5GENIChomozygous137986881
7661050661051AG5GENIChomozygous137986882
7663535663536GA29GENIChomozygous137986883
7664249664250TC15GENIChomozygous137986884
7665390665391TA16GENIChomozygous137986885
7666522666523CT10GENIChomozygous137986886
7669983669984TC17GENIChomozygous137986887
7670505670506GT16GENIChomozygous137986888
7670556670556G17GENIChomozygous137932171
7660967660968A14GENIChomozygous137932170
7669078669079C7GENICheterozygous403198043
7669073669074GA7GENIChomozygous403198040
7669073669074G7GENICheterozygous403198041
7669078669079CG7GENIChomozygous403198042
7670611670612AG18GENIChomozygous137986889
7670612670613GC18GENIChomozygous137986890
7670614670615TC20GENIChomozygous137986891
7670889670890TC24GENIChomozygous137986892
7672074672075TC18GENIChomozygous137986893
7672496672497TC21GENIChomozygous137986894
7672674672675T19GENIChomozygous137932172
7672727672728AG19GENIChomozygous137986896
7672752672753AG21GENIChomozygous137986897
7672871672872GC21GENIChomozygous137986898
7673085673086TG18GENIChomozygous137986899
7673168673169TC19GENIChomozygous137986900
7673879673880GA17GENICpossibly homozygous137986901
7673935673935TG19GENIChomozygous137932173
7674344674345TC11GENIChomozygous137986902
7674865674865CT5GENIChomozygous137932174
7675508675508A20GENIChomozygous137932175
7676176676177AG16GENIChomozygous137986903
7676656676657GA37GENIChomozygous137986904
7676986676987CA24GENIChomozygous137986905
7677062677063AG29GENIChomozygous137986906
7677412677413AG21GENIChomozygous137986907
7677928677929GA24GENIChomozygous137986908
7677953677954GA23GENIChomozygous137986909
7677993677994TC26GENIChomozygous137986910
7678006678007GA26GENIChomozygous137986911
7678075678076GA20GENIChomozygous137986912
7678100678101CG19GENIChomozygous137986913
7674710674712CC3GENIChomozygous148226967