chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC25GENIChomozygous51371746
102640261126402612CT30GENIChomozygous51371748
102640292126402922AAT24GENIChomozygous51371750
102640297526402976TTTTATTTTATAGCACTACTAGGTCATCCTGTAAAGGACTTTGCATGTTGC32GENIChomozygous52362382
102640309326403094TG30GENIChomozygous51371752
102640313226403133TC29GENIChomozygous51371754
102640317126403172TTCAGCTACTGCTCATTG38GENIChomozygous51371756
102640334626403347A-19GENIChomozygous51371758
102640385526403859ACTT----17GENICpossibly homozygous51371762
102640489226404893GA25GENIChomozygous51371763
102640495526404956CA30GENIChomozygous51371765
102640597626405977AC14GENIChomozygous51371767
102640742226407423AG17GENIChomozygous51371769
102640806226408063AG30GENIChomozygous51371771
102640920926409210TC33GENIChomozygous51371773
102641095726410959CA--2GENIChomozygous52362384
102641504726415048CA24GENIChomozygous51371779
102641564926415650AACAAGCT11GENIChomozygous51371781
102641577026415771CG7GENIChomozygous51371783
102641580026415801TC10GENIChomozygous51371785
102641608926416090AATCTTT25GENIChomozygous51371791
102641647326416474CT28GENIChomozygous51371793
102641661126416612TC27GENIChomozygous51371795
102641739226417393TTACACAC3GENICheterozygous52362388
102641739226417393TTACACACAC3GENICheterozygous52362390
102641798026417981GA27GENIChomozygous51371797
102641817926418180AG26GENIChomozygous51371799
102641847526418476GC23GENIChomozygous51371801
102641859826418604AGTAAA------31GENIChomozygous51371803
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------19GENIChomozygous51371805
102641860426418605AC32GENIChomozygous52315103
102641581026415811CCTCTCTCTTTCTTTCTT1GENIChomozygous52797491