chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124046651440466518ATTT----24GENIChomozygous50203597
124046653140466532AATGCG9GENIChomozygous50203599
124046653940466540AG23GENIChomozygous50203600
124046770740467716TCTGTTGTT---------15GENIChomozygous50203601
124046785940467860AG15GENIChomozygous50203602
124046797040467971CCT2GENIChomozygous50203603
124046806340468064GA11GENIChomozygous50203604
124046844640468447GC16GENIChomozygous50203605
124046945240469453TA22GENIChomozygous50203607
124046960240469603CA21GENIChomozygous50203608
124047081540470816T-5GENICheterozygous50203609
124047088840470889CT13GENIChomozygous50203610
124047611140476112T-13GENIChomozygous50203611
124047621040476211CA24GENIChomozygous50203612
124047621140476212TC23GENIChomozygous50203613
124047652540476526AC17GENIChomozygous50203614
124048032340480324GT11GENIChomozygous50203615
124048126240481263GGAAA23GENIChomozygous50203616
124048310240483103CA26GENIChomozygous50203617
124048607840486079CCT12GENIChomozygous50203618
124048648340486484T-19GENIChomozygous50203621
124048648740486488TC18GENIChomozygous50203622
124048649040486491GT18GENIChomozygous50203623
124048651440486515TC19GENIChomozygous50203624
124048652540486526AT19GENIChomozygous50203625
124048654940486550GA16GENIChomozygous50203626
124048655340486554GT18GENIChomozygous50203627
124048658240486583TTG22GENIChomozygous50203628
124048658740486588A-27GENIChomozygous50203629
124048664240486643TTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCG17GENIChomozygous50592130
124048667140486672CCTG29GENIChomozygous50203633
124048689440486904ACACACACAC----------9GENIChomozygous50203634
124048700640487007CT15GENIChomozygous50203635
124048842740488428GA28GENIChomozygous50203636
124048982940489830TC32GENIChomozygous50203637
124049009140490092TC26GENIChomozygous50203638
124049033440490335CCTGTT25GENIChomozygous50203639
124049091540490916TC34GENIChomozygous50203640
124049249240492493GA15GENIChomozygous50203641
124049297540492976AG10GENIChomozygous50203642
124049372240493723AT22GENIChomozygous50203643
124049458640494594TGATGTTT--------15GENIChomozygous50203644
124049459540494597TT--14GENIChomozygous50203645
124049654840496549GA12GENIChomozygous50203646
124049671140496712AG23GENIChomozygous50203647
124049689340496894CT19GENIChomozygous50203648
124049797740497978GA19GENIChomozygous50203649
124049800640498007TA23GENIChomozygous50203650
124049812840498129CT32GENIChomozygous50203651
124049812940498130AG32GENIChomozygous50203652
124049839040498391CCA19GENICpossibly homozygous50203653
124049859540498596AG22GENIChomozygous50203654
124049868240498721CCATGCCAGGCTCACTTCACTCTGGGTCCCTTCTACTGT---------------------------------------15GENIChomozygous50543637
124048628540486289ACAA----12GENIChomozygous50763026
124049451240494513CCACA23GENICheterozygous50615532