chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124046651440466518ATTT----12GENIChomozygous50203597
124046653140466539ATGCGTGC--------7GENIChomozygous50203598
124046718640467187GA13GENIChomozygous50422685
124046723340467234A-8GENIChomozygous50422686
124046728640467287GT22GENIChomozygous50422687
124046770740467716TCTGTTGTT---------15GENIChomozygous50203601
124046792840467929A-14GENIChomozygous50422688
124046806340468064GA9GENIChomozygous50203604
124046830840468309TC14GENIChomozygous50422689
124046844640468447GC21GENIChomozygous50203605
124046895340468954CA18GENIChomozygous50422690
124046910040469103AAA---10GENICheterozygous50558979
124046910140469103AA--10GENICpossibly homozygous50543630
124046917040469176TTTTTT------1GENIChomozygous50599320
124046945240469453TA13GENIChomozygous50203607
124047088840470889CT16GENIChomozygous50203610
124047611140476112T-20GENIChomozygous50203611
124047621040476211CA18GENIChomozygous50203612
124047621140476212TC18GENIChomozygous50203613
124047652540476526AC21GENIChomozygous50203614
124047674740476748GGA13GENICpossibly homozygous50422693
124047679540476805TTTTTTTTGT----------9GENIChomozygous50543631
124047701640477018GT--2GENIChomozygous50600910
124048094540480946TA26GENIChomozygous50543632
124048094640480947AT28GENIChomozygous50543633
124048121940481220GA28GENIChomozygous50422694
124048221240482213GA18GENIChomozygous50422695
124048310240483103CA13GENIChomozygous50203617
124048579540485807ACACACACACAC------------2GENIChomozygous50600911
124048607840486079CCT10GENIChomozygous50203618
124048627240486273TTACATACAA9GENIChomozygous50543634
124048648340486484T-33GENIChomozygous50203621
124048648740486488TC34GENIChomozygous50203622
124048649040486491GT33GENIChomozygous50203623
124048651440486515TC26GENIChomozygous50203624
124048652540486526AT25GENIChomozygous50203625
124048654940486550GA18GENIChomozygous50203626
124048655340486554GT20GENIChomozygous50203627
124048658240486583TTG13GENIChomozygous50203628
124048658740486588A-12GENIChomozygous50203629
124048662540486626GGTGTCTGTCTGTCTGTC9GENICpossibly homozygous50543635
124048667140486672CCTG16GENIChomozygous50203633
124048690040486904ACAC----6GENIChomozygous50543636
124048700640487007CT25GENIChomozygous50203635
124048842740488428GA23GENIChomozygous50203636
124048892540488926CA12GENIChomozygous50422696
124048982940489830TC25GENIChomozygous50203637
124049009140490092TC18GENIChomozygous50203638
124049033440490335CCTGTT17GENIChomozygous50203639
124049091540490916TC11GENIChomozygous50203640
124049249240492493GA22GENIChomozygous50203641
124049280840492809AG10GENICpossibly homozygous50422697
124049297540492976AG12GENIChomozygous50203642
124049400840494009TC23GENIChomozygous50422698
124049452040494521TA16GENIChomozygous50422699
124049557640495577GA17GENIChomozygous50422700
124049654840496549GA15GENIChomozygous50203646
124049713440497135CT17GENIChomozygous50422701
124049722040497221GA15GENIChomozygous50422702
124049797740497978GA14GENIChomozygous50203649
124049800640498007TA15GENIChomozygous50203650
124049812840498129CT15GENIChomozygous50203651
124049812940498130AG15GENIChomozygous50203652
124049839040498391CCA15GENIChomozygous50203653
124049859540498596AG21GENIChomozygous50203654
124049868240498721CCATGCCAGGCTCACTTCACTCTGGGTCCCTTCTACTGT---------------------------------------7GENIChomozygous50543637