chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85355184653551847CT2GENIChomozygous52633577
85355186853551869AG11GENIChomozygous52633579
85355209953552100GT22GENIChomozygous52633581
85355303653553045AATGATGGT---------4GENIChomozygous52633583
85355309453553095GGA8GENICheterozygous52633585
85355323053553231GT10GENIChomozygous52633587
85355323453553235GA8GENIChomozygous52633589
85355324153553242CA8GENICpossibly homozygous52633591
85355338753553388A-3GENICheterozygous52633593
85355387453553875TC14GENIChomozygous52633595
85355399053553993AAC---5GENIChomozygous52633597
85355424353554244CT7GENIChomozygous52633615
85355458353554597TTTAAAGGAAAATA--------------5GENICheterozygous53387277
85355459953554600GGT2GENIChomozygous52633625
85355465053554651TC12GENIChomozygous52633627
85355501453555015AT20GENICpossibly homozygous52633629
85355541053555411AAC14GENICpossibly homozygous53363848
85355592853555929AC19GENIChomozygous52633631
85355600953556010AG8GENIChomozygous52633633
85355606053556061AT10GENIChomozygous52633635
85355608253556083GGA11GENIChomozygous52633637
85355614253556143CT12GENIChomozygous52633639
85355630453556305CT17GENICpossibly homozygous52633641
85355644253556443GA8GENIChomozygous52633643
85355644453556445CT8GENIChomozygous52633645
85355653053556531AG5GENICheterozygous52633647
85355670853556709CT26GENICpossibly homozygous52633649
85355709653557097TA30GENIChomozygous52633651
85355741053557411CT23GENICpossibly homozygous52633653
85355753653557537GA16GENICpossibly homozygous52633655
85355761353557614GA13GENICpossibly homozygous52633657
85355816453558165GA16GENICpossibly homozygous52976398