chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121450732145075TG53GENIChomozygous135390235
121453842145385CA19GENIChomozygous135482880
121453862145387CT18GENIChomozygous135482881
121456432145644GA29GENIChomozygous135482882
121457272145728GA40GENIChomozygous135482883
121457432145744GA44GENIChomozygous135482884
121465772146578GA37GENIChomozygous135482885
121469592146960CG38GENIChomozygous135482886
121478092147810CT52GENIChomozygous135482887
121482462148247AG48GENIChomozygous135482888
121499792149980AT51GENIChomozygous135482889
121509642150965AT51GENIChomozygous135482890
121523182152319CT65GENIChomozygous135482891
121529052152906GA49GENIChomozygous135482892
121532042153207AAA57GENIChomozygous135390239
121456002145600AAAAC25GENIChomozygous135390236
121470212147045TACATCCTCCTGAATTATTCTGTT40GENIChomozygous135390237
121477722147772A47GENICpossibly homozygous135390238
121533352153336CT43GENIChomozygous135482893
121544462154447TC40GENIChomozygous135482894
121544622154463CT42GENIChomozygous135482895
121545682154569AT52GENICpossibly homozygous135482896
121549622154963CT44GENIChomozygous135482897
121550392155040GA51GENIChomozygous135482898
121555082155509TG43GENIChomozygous135482899
121555982155599CT46GENIChomozygous135482900
121556652155666TC55GENIChomozygous135482901
121560902156091TG64GENIChomozygous135482902
121561942156203TTATTTTAA33GENIChomozygous135390240
121562372156238AG35GENIChomozygous135482903
121565042156504TC23GENICpossibly homozygous135390241
121453932145394A17GENICheterozygous402938830
121453932145394AT17GENICheterozygous402938831
121453932145394AC17GENICheterozygous402938832
121565082156508TC19GENIChomozygous135390242
121568002156800AAGTTG38GENIChomozygous135390243
121574142157415TC48GENIChomozygous135482904
121577802157781GC51GENIChomozygous135482905