chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
33743472137434722AG22GENIChomozygous112109164
33743493937434940GA26GENIChomozygous112109166
33743507637435077AC35GENIChomozygous112109168
33743508737435088AG34GENIChomozygous112109170
33743601537436016AT21GENIChomozygous111545715
33743601637436017AT19GENIChomozygous111545716
33743620337436204AG20GENIChomozygous112109172
33743632637436327CT21GENIChomozygous112109174
33743702437437025AC31GENIChomozygous112109176
33743737537437376GA29GENIChomozygous112109178
33743774537437746GA25GENIChomozygous112109180
33743800137438002CG11GENIChomozygous112109182
33743859537438596CG9GENICheterozygous112109184
33743867337438674GA15GENICpossibly homozygous112109186
33743873837438739GA23GENIChomozygous112109188
33743939337439394CG17GENIChomozygous112109190
33743986037439861GA12GENIChomozygous112109192
33743987437439875AG13GENIChomozygous112109193
33743995337439954AG7GENIChomozygous112109195
33744137237441373AG29GENIChomozygous112109197
33744142637441427TC26GENIChomozygous112109199
33744152937441530TC23GENIChomozygous112109201
33744162237441623GA26GENIChomozygous112109203
33744169237441693TC19GENIChomozygous112109205
33744169737441698CG20GENIChomozygous112109207
33744214637442147CG17GENIChomozygous112109209
33744215237442153AG15GENIChomozygous112109211
33744249437442495AC24GENIChomozygous112109213
33744272937442730CA28GENIChomozygous112109215
33744316937443170TC25GENIChomozygous112109217
33744457337444574AC19GENIChomozygous111545717
33744458937444590GA17GENIChomozygous112109219
33744473837444739GA2GENIChomozygous112109221
33744482037444821CT11GENIChomozygous111545718
33744555737445558CT23GENICpossibly homozygous112109223
33744562037445621AC14GENIChomozygous112109225
33744639237446393AG19GENIChomozygous112109231
33744602737446028AC9GENIChomozygous112109227
33744603937446040AG10GENIChomozygous112109229