chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124919514249195143TG18GENIChomozygous50231842
124920070849200712CACA----5GENICheterozygous50231881
124920134649201347GGCACACA6GENIChomozygous50546650
124919630749196308TTAC23GENIChomozygous50343706
124919733549197336TTTGG8GENIChomozygous50546645
124919733649197337CG8GENIChomozygous50546646
124919733949197340AT6GENIChomozygous50546647
124919734749197348AAGCTCAGTGGTAGAGCGCTTGCCTAGC3GENIChomozygous50546648
124919734949197350AAGC3GENIChomozygous50546649
124920071049200712CA--5GENICheterozygous50413474
124920617949206181CA--14GENICpossibly homozygous50413476
124920660449206605AG25GENIChomozygous50491967
124920477049204771CA8GENIChomozygous50491959
124920511449205118AAAA----13GENIChomozygous50491961
124920703649207037AAT8GENICheterozygous50575706
124920736149207362CCT15GENIChomozygous50491969
124921063049210646TCTCTCTTTCTCTGTC----------------8GENIChomozygous50546651
124921152749211529GG--6GENIChomozygous50491973
124921277649212777G-11GENIChomozygous50231971
124921570249215703T-10GENICheterozygous50231987
124922053349220579TTTATAGCGAATCAGGCACACCTGGCTGTTTGTTGCCAGGTAACTG----------------------------------------------10GENICpossibly homozygous50546652
124922484149224843AC--1GENIChomozygous50565999
124922440149224402T-4GENIChomozygous50387973
124922190349221904C-5GENIChomozygous50470670