chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86971096269710963GA19GENIChomozygous53469466
86971159669711597CA18GENIChomozygous53469474
86971159869711599TC17GENIChomozygous53469476
86971178069711781CA18GENICheterozygous53515609
86971224569712246GA24GENIChomozygous53965495
86971275669712757CG28GENIChomozygous53965498
86971301669713017GT24GENIChomozygous53515613
86971342569713426CT14GENIChomozygous53469478
86971421169714212A-18GENIChomozygous53364291
86971458069714581CA12GENIChomozygous53515615
86971495769714958TC13GENIChomozygous53364292
86971567269715673TC21GENIChomozygous53515619
86971628769716288GA29GENIChomozygous53515625
86971648969716490TTGTCTAG29GENIChomozygous53515627
86971780469717809GTGGG-----11GENIChomozygous53618605
86971784169717842TC14GENIChomozygous53515631
86971801469718015GA26GENIChomozygous53965500
86971816269718172GTGTGTGTGT----------11GENICheterozygous53469484
86971816469718172GTGTGTGT--------11GENICheterozygous53469486
86971844269718443AC22GENIChomozygous53515633
86971927569719276CT27GENICpossibly homozygous53515635
86971932769719328CT25GENIChomozygous53515637
86972068969720690GC19GENIChomozygous53965502
86972095369720954TC19GENIChomozygous53469489
86971721069717211TTAG20GENIChomozygous52673104
86971784269717843GGC14GENIChomozygous52673105