chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43206793432067935TC107GENICheterozygous119584647
43207908932079090TC68GENIChomozygous112569432
43207061632070617CT68GENIChomozygous112569420
43207768832077689AC41GENIChomozygous112569422
43207810332078104CT36GENIChomozygous112569424
43207821632078217CG45GENIChomozygous112569426
43207840332078404CT52GENIChomozygous112569428
43207840532078406GA52GENIChomozygous112569430
43207266232072662ACAGGTTA55GENIChomozygous128019190
43207744532077445A61GENIChomozygous128019191
43207811032078112TA35GENIChomozygous128019192
43207897032078971A70GENIChomozygous128019193
43207806732078067CATATATATATATATATA21GENICheterozygous129901403
43207912632079127TA60GENIChomozygous112569434
43208098532080988AGA9GENIChomozygous128019194
43208127332081273AAG70GENIChomozygous128019195
43208135832081359TC84GENIChomozygous112569436
43208205932082060GA36GENIChomozygous112569438
43208230232082303AG34GENIChomozygous112569440
43208309332083094AG65GENIChomozygous112569442
43208388732083888TC59GENIChomozygous112569444
43208392832083929AC61GENIChomozygous112569446
43208412932084130GA71GENIChomozygous112569448
43208419232084193GC68GENIChomozygous112569450
43208466632084667CT74GENIChomozygous112569452
43208468732084688CT70GENIChomozygous112569454
43208485932084860CT65GENIChomozygous112569456
43208507632085079AAA61GENIChomozygous128019196
43208521032085211AG64GENIChomozygous112569458
43208521432085215TA64GENIChomozygous112569460
43208530532085306AC59GENIChomozygous112569462
43208531832085319A58GENIChomozygous128019197
43208593232085933GA62GENICpossibly homozygous112569464
43208627932086281AT64GENIChomozygous128019198
43208755332087554AG49GENIChomozygous112569466