chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102986838129868382TC21GENIChomozygous67838499
102986858129868582CT29GENIChomozygous67838504
102987003729870038CT33GENIChomozygous67838508
102987013729870138AG34GENIChomozygous67838512
102987019729870198GA32GENIChomozygous67838516
102987061029870611CT25GENIChomozygous67838520
102987063429870635TC23GENIChomozygous67838525
102987092429870925TC30GENIChomozygous67838529
102987099129870992TC31GENICpossibly homozygous67838533
102987119729871198GT31GENIChomozygous67838537
102987416729874168AG6GENIChomozygous67838551
102987463329874634GT20GENIChomozygous67838555
102987555129875552AT30GENIChomozygous67838559
102987562629875627CT32GENIChomozygous67838562
102987586829875869CT16GENIChomozygous67838566
102987658629876587TC34GENIChomozygous67838570
102987686829876869CT34GENIChomozygous67838574
102987891829878919GA27GENIChomozygous67838578
102988069829880699TC21GENIChomozygous67838582
102988095529880956GA29GENIChomozygous67838585