chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107519609975196100G-14GENIChomozygous710885463
107519701475197015TC26GENIChomozygous570168691
107519744275197443TC19GENIChomozygous570168692
107519886475198865AG12GENIChomozygous570168693
107520110875201109CT26GENIChomozygous571916584
107520167575201676A-13GENIChomozygous710885464
107520670675206707CCTCTCTCTCTCTCTT7GENICheterozygous710885465
107520672975206737TCTCTCTC--------6GENIChomozygous710885468
107520689775206909AGTGGCAGTGGC------------6GENIChomozygous710885470
107520781175207812TC3GENIChomozygous571916585
107520806775208068CCT5GENICheterozygous710885471
107520816075208161AG5GENIChomozygous571916586
107520817675208177TC9GENIChomozygous571916587
107520930575209306TC23GENIChomozygous571916588
107521038575210386TC26GENIChomozygous570168694
107521095775210958GC7GENIChomozygous571916589
107521109975211100GA16GENIChomozygous571916590
107521167075211671AAGG4GENIChomozygous710885473
107521207075212072AG--7GENIChomozygous710885474
107521219375212194GA10GENIChomozygous571916591
107521260675212607GT2GENIChomozygous571916592
107521283875212839CCCA6GENIChomozygous710885475
107521307575213076AAT21GENIChomozygous710885476
107521309275213093GC21GENIChomozygous570168695
107521405075214051AATT10GENIChomozygous710885477