chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4233144018233144019GC6GENIChomozygous58098349
4233144806233144807TTA6GENIChomozygous58098351
4233144956233144957GA3GENIChomozygous58098353
4233145055233145056TC6GENIChomozygous58098355
4233145066233145067TC5GENIChomozygous58098357
4233146470233146471GA6GENIChomozygous58098359
4233146505233146506CT5GENIChomozygous58098361
4233147797233147798GA2GENIChomozygous58098365
4233148073233148074AAAT6GENIChomozygous58098367
4233148249233148250CCT6GENIChomozygous58098369
4233148377233148378TG8GENIChomozygous58098371
4233148410233148411GC6GENIChomozygous58098373
4233148791233148792TTA4GENIChomozygous58098375
4233149677233149678A-3GENIChomozygous57132967
4233149850233149851CCA5GENIChomozygous57132969
4233149897233149898CCA4GENIChomozygous57132971
4233151420233151421AG9GENIChomozygous58098377
4233152532233152533CT7GENIChomozygous58098379
4233152577233152578TC8GENIChomozygous57132975
4233152627233152628TC6GENIChomozygous58098381
4233152761233152762GC10GENIChomozygous58098383
4233152778233152779AAT7GENIChomozygous57132977
4233153129233153130GA5GENIChomozygous58098385
4233153317233153318CT4GENIChomozygous58098387
4233153344233153345GA2GENIChomozygous58098389
4233154324233154325CT9GENIChomozygous57132980
4233155240233155241TC9GENIChomozygous57132982
4233148049233148050TTTATATA2GENIChomozygous57371078
4233152644233152647ATT---2GENIChomozygous58411665
4233148149233148165ATCTATCTATCTATCT----------------4GENIChomozygous58379932
4233151472233151479ATTATTA-------6GENIChomozygous58379934