chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110442260110442261TG26GENICpossibly homozygous112292297
3110442262110442263TG25GENIChomozygous112292299
3110443278110443279CA12GENIChomozygous119739758
3110443548110443549GT11GENIChomozygous111672841
3110452494110452495TC18GENIChomozygous112292305
3110453246110453247GA26GENIChomozygous112292307
3110453430110453431AG19GENIChomozygous112292309
3110453556110453557AG17GENIChomozygous112292311
3110454023110454024CT17GENIChomozygous112292313
3110454715110454716AG25GENIChomozygous112138906
3110456058110456059AT26GENIChomozygous112292317
3110456080110456081GA29GENIChomozygous112292319
3110463051110463052GA32GENIChomozygous112138911
3110463066110463067AG32GENIChomozygous111672857
3110462720110462721GA26GENIChomozygous112003593
3110465091110465092TC25GENIChomozygous112003601
3110465447110465448AG24GENIChomozygous112003603
3110466543110466544CT24GENIChomozygous112003605
3110467748110467749GC25GENIChomozygous112003607
3110469248110469249TC25GENIChomozygous112003609
3110469574110469575AG29GENIChomozygous112138912
3110474591110474592TC16GENIChomozygous112003617
3110476491110476492GA22GENIChomozygous112138914
3110480114110480115GT26GENIChomozygous112003627
3110481041110481042GA25GENIChomozygous112003629
3110481403110481404TC24GENIChomozygous112003631
3110481916110481917CT29GENIChomozygous112003635
3110482841110482842AG28GENIChomozygous111672861