chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107519609975196100G-34GENIChomozygous708811837
107519701475197015TC16GENIChomozygous566798395
107519744275197443TC11GENIChomozygous566798396
107519886475198865AG15GENIChomozygous566798397
107520110875201109CT13GENIChomozygous568571000
107520167575201676A-8GENIChomozygous708811838
107520670675206707CCTCTCTCTCTCTCTT6GENICheterozygous708811839
107520672975206737TCTCTCTC--------10GENICheterozygous708811842
107520673175206737TCTCTC------10GENICheterozygous708811841
107520689775206909AGTGGCAGTGGC------------12GENIChomozygous708811844
107520781175207812TC11GENIChomozygous568571001
107520806775208068CCT6GENICheterozygous708811845
107520816075208161AG14GENIChomozygous568571002
107520817675208177TC17GENIChomozygous568571003
107520930575209306TC31GENIChomozygous568571004
107521038575210386TC29GENIChomozygous566798398
107521095775210958GC14GENIChomozygous568571005
107521109975211100GA16GENIChomozygous568571006
107521167075211671AAGG9GENIChomozygous708811847
107521207075212072AG--17GENIChomozygous708811848
107521219375212194GA10GENIChomozygous568571007
107521260675212607GT6GENIChomozygous568571008
107521283875212839CCCA19GENIChomozygous708811849
107521307575213076AAT13GENIChomozygous708811850
107521309275213093GC19GENIChomozygous566798399
107521405075214051AATT7GENIChomozygous708811851