chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63410536234105363G1GENIChomozygous133402976
63410536634105367GT1GENIChomozygous133404503
63410536934105371GT1GENIChomozygous130660395
63410537534105376GT3GENIChomozygous130662704
63410537734105387GCGCCCGGCG3GENIChomozygous130660396
63410538834105389CT3GENIChomozygous118710133
63410539034105390T4GENIChomozygous130660397
63410539534105395C5GENIChomozygous130660398
63410540134105402G5GENIChomozygous130660399
63410540734105407T6GENIChomozygous130660400
63410542134105422GT8GENIChomozygous118710136
63410542234105423TC8GENIChomozygous130662705
63410543234105433CA11GENIChomozygous130662706
63410543334105434AC11GENIChomozygous130662707
63410544634105447T12GENIChomozygous130660401
63410823934108246AACAGCA22GENIChomozygous128328746
63411668734116688TC9GENIChomozygous114756960
63411671934116720C5GENICheterozygous128328747
63411672934116730AT5GENICheterozygous128413016
63411695634116957TC8GENICheterozygous134423970
63411695934116960GA8GENICheterozygous134423971
63411696234116963AT8GENICheterozygous134423972
63411703834117039AC9GENICheterozygous129931282
63411735534117356GC4GENICheterozygous134423973
63412078734120787T25GENIChomozygous128328748
63414872134148722C21GENIChomozygous128328749
63414873134148731AG21GENIChomozygous128328750
63414874434148745CA17GENIChomozygous114756968
63414874734148747G16GENIChomozygous128328751
63414875134148751G15GENIChomozygous128328752
63414875634148756GA14GENIChomozygous128328753
63414876734148767G11GENIChomozygous128328754
63414877434148774G7GENIChomozygous128328755
63414878334148783GAG7GENIChomozygous128328756
63414879434148795CG3GENIChomozygous128413031
63414879934148799T2GENIChomozygous128328757
63414880434148804G1GENIChomozygous128328758
63414881034148817GGGAAGG2GENIChomozygous128328759
63414883434148834G4GENIChomozygous128328760
63414883834148838G4GENIChomozygous128328761
63412078734120788GC25GENIChomozygous118552905