chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122703848527038486CA25GENIChomozygous50373978
122703874027038741GA22GENIChomozygous50467379
122703878827038789GT22GENIChomozygous50373982
122703881727038818TC22GENIChomozygous50419802
122703883027038831CT21GENIChomozygous50373984
122703962227039623CT26GENIChomozygous50151594
122704038227040384TT--15GENIChomozygous50151598
122704102727041028AG39GENIChomozygous50151600
122704197027041971AAT16GENICheterozygous50151602
122704197027041971AATT16GENICpossibly homozygous50151604
122704217427042175TTTG5GENIChomozygous50151608
122704374227043743TC18GENIChomozygous50151617
122704383127043832CCTG5GENICheterozygous50374004
122704387727043878CCTGTG7GENICpossibly homozygous50440445
122704390427043905CCGT12GENIChomozygous50405783
122704470127044702AG19GENIChomozygous50151627
122704478427044785AG18GENIChomozygous50151629
122704511527045116GA22GENIChomozygous50467381
122704577527045776AG24GENIChomozygous50151631
122704630527046306CT33GENIChomozygous50467383
122704681627046817G-33GENIChomozygous50467385
122704794127047942C-9GENICheterozygous50151641
122704881827048819AT38GENIChomozygous50440449
122704892027048921CT22GENIChomozygous50467387
122704893027048931AAG19GENIChomozygous50151651
122704903627049037GT24GENIChomozygous50151653
122704911427049115CCTCGTGAGCGAG27GENIChomozygous50151655
122704914727049148AG38GENIChomozygous50151659
122705011327050114GA26GENIChomozygous50419806
122705062927050630C-23GENIChomozygous50151663
122705067027050671CT25GENIChomozygous50467389
122705089227050893CCA13GENIChomozygous50151665
122705089327050894GGGCTGTGCATGGAAAAA13GENIChomozygous50151667
122705110827051109CT15GENIChomozygous50467391
122705111827051119GC16GENIChomozygous50419807
122705143227051433CT27GENIChomozygous50419809
122705186527051866GA22GENIChomozygous50405795
122705224927052250CT16GENIChomozygous50419810
122705237027052371A-17GENIChomozygous50405797
122705238527052386AG20GENIChomozygous50539515
122705257427052575CT28GENICpossibly homozygous50467393
122705271027052711CCTATG3GENIChomozygous50151683
122705332327053324GA22GENIChomozygous50467395
122705385327054058GGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGGGAGGGGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCTGGGGGTGTGGCTCAGTGGTAGAGCACCTGCCTAGAATCCCCCAGTGAGGGGCTGGGGGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCTGGG-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------22GENICheterozygous50509512
122705410027054153GAGGGGCTGGGGGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGT-----------------------------------------------------6GENICheterozygous50654666
122705471827054719CA22GENIChomozygous50467397
122705600827056012AAAA----3GENIChomozygous50539516
122705729827057299AG33GENIChomozygous50151743
122705952527059526TC10GENIChomozygous50151767
122706008227060094CCTCCCTCCCTC------------1GENIChomozygous50608309
122706197527061981GTTGTC------27GENIChomozygous50151793
122706200327062004GA28GENIChomozygous50467401
122706260727062608GA17GENIChomozygous50467403
122706580127065802GA20GENIChomozygous50151837
122706584627065847GC20GENIChomozygous50151839
122706587127065872C-15GENIChomozygous50374051
122706588527065886TA17GENIChomozygous50467405
122706621327066214CA19GENIChomozygous50151843
122706688827066889CT31GENIChomozygous50151847
122706729427067295T-17GENICpossibly homozygous50151849
122706741027067411GA25GENIChomozygous50467407