chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC24GENIChomozygous51371746
102640261126402612CT21GENIChomozygous51371748
102640292126402922AAT12GENIChomozygous51371750
102640309326403094TG13GENIChomozygous51371752
102640313226403133TC7GENIChomozygous51371754
102640317126403172TTCAGCTACTGCTCATTG1GENIChomozygous51371756
102640334626403347A-1GENIChomozygous51371758
102640379526403796GA9GENICheterozygous51371760
102640385526403859ACTT----5GENICheterozygous51371762
102640489226404893GA13GENIChomozygous51371763
102640495526404956CA12GENIChomozygous51371765
102640597626405977AC10GENIChomozygous51371767
102640742226407423AG12GENIChomozygous51371769
102640806226408063AG16GENIChomozygous51371771
102640920926409210TC8GENIChomozygous51371773
102641095126410953CA--2GENIChomozygous51633140
102641504726415048CA5GENIChomozygous51371779
102641564926415650AACAAGCT1GENIChomozygous51371781
102641577026415771CG6GENICheterozygous51371783
102641580026415801TC8GENICheterozygous51371785
102641580926415811TC--5GENICheterozygous51371787
102641581426415815TC7GENICheterozygous51371789
102641608926416090AATCTTT5GENIChomozygous51371791
102641647326416474CT8GENIChomozygous51371793
102641661126416612TC9GENIChomozygous51371795
102641798026417981GA19GENIChomozygous51371797
102641817926418180AG18GENICpossibly homozygous51371799
102641847526418476GC17GENIChomozygous51371801
102641859826418604AGTAAA------8GENICpossibly homozygous51371803
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------2GENIChomozygous51371805