chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4233144018233144019GC12GENIChomozygous58098349
4233144806233144807TTA15GENIChomozygous58098351
4233144956233144957GA9GENIChomozygous58098353
4233145055233145056TC14GENIChomozygous58098355
4233145066233145067TC15GENIChomozygous58098357
4233146470233146471GA14GENIChomozygous58098359
4233146505233146506CT7GENIChomozygous58098361
4233147797233147798GA3GENICheterozygous58098365
4233148049233148050TTTA5GENICheterozygous57132958
4233148073233148074AAAT3GENICheterozygous58098367
4233148249233148250CCT4GENIChomozygous58098369
4233148377233148378TG3GENIChomozygous58098371
4233148410233148411GC3GENIChomozygous58098373
4233148791233148792TTA3GENIChomozygous58098375
4233149677233149678A-10GENIChomozygous57132967
4233149850233149851CCA14GENIChomozygous57132969
4233149897233149898CCA14GENIChomozygous57132971
4233151420233151421AG7GENIChomozygous58098377
4233152532233152533CT7GENICpossibly homozygous58098379
4233152577233152578TC7GENIChomozygous57132975
4233152627233152628TC6GENIChomozygous58098381
4233152761233152762GC8GENIChomozygous58098383
4233152778233152779AAT7GENIChomozygous57132977
4233153129233153130GA10GENIChomozygous58098385
4233153317233153318CT12GENIChomozygous58098387
4233153344233153345GA11GENIChomozygous58098389
4233154324233154325CT13GENIChomozygous57132980
4233155240233155241TC10GENIChomozygous57132982
4233148049233148050TTTATATA5GENICheterozygous57371078
4233152644233152647ATT---1GENIChomozygous58411665
4233148149233148165ATCTATCTATCTATCT----------------3GENIChomozygous58379932
4233151472233151479ATTATTA-------1GENIChomozygous58379934