chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118799010687990107AG16GENIChomozygous115929583
118799218687992187GC18GENIChomozygous115929585
118799262787992628TC32GENIChomozygous115929587
118799387087993871CT18GENIChomozygous115929589
118799417987994180TC22GENIChomozygous115929591
118799531187995312AT14GENIChomozygous115929593
118799588487995885AG19GENIChomozygous116110827
118799651987996520CT7GENIChomozygous115929595
118799774087997741TA16GENIChomozygous115929597
118799789787997898GA20GENIChomozygous115929599
118799900087999001GC26GENIChomozygous115929601
118799939787999398AG25GENIChomozygous115929603
118799944587999446CT36GENIChomozygous115929605
118799981987999820CA5GENIChomozygous126285262
118800033188000332GA20GENIChomozygous115929607
118800057288000573GT24GENIChomozygous115929609
118800091588000916AG26GENIChomozygous115929611
118800116788001168GA12GENICheterozygous115929613
118800277488002775AG25GENIChomozygous115929615
118800346088003461GT18GENIChomozygous115929617
118800409688004097AG18GENIChomozygous115929619
118800508988005090TA24GENIChomozygous115929621
118800647888006479TG18GENIChomozygous115929623
118800876288008763GA23GENIChomozygous115929627
118800992388009924GA24GENIChomozygous115929629
118801015988010160CT21GENIChomozygous115929631
118801121188011212GA25GENIChomozygous115929633
118801233588012336AG5GENIChomozygous116400622
118801319388013194AT10GENIChomozygous115929639
118801321188013212CT10GENIChomozygous115929641
118801339288013393GA29GENIChomozygous115929643