chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102902959729029598TC38GENIChomozygous116864753
102903116029031161AT9GENIChomozygous117120932
102903546029035461CT74GENIChomozygous116539022
102903027129030272TG37GENIChomozygous116539016
102903283429032835TG29GENIChomozygous116539018
102903478429034785GA26GENIChomozygous116539020
102903621429036215AG45GENIChomozygous116539024
102903704429037045TC45GENIChomozygous116539026
102903777129037772AG61GENIChomozygous116539028
102903785029037851GA47GENIChomozygous116539030
102903796329037964AG32GENIChomozygous116539032
102903796429037965CT32GENIChomozygous116539034
102903796629037967CT32GENIChomozygous116539036
102903796929037970GA34GENIChomozygous116539038
102903803229038033GA76GENICpossibly homozygous116539040
102903888829038889TC37GENIChomozygous116539042
102903993129039932AG55GENIChomozygous116539044
102904011329040114CT71GENIChomozygous116539046
102904068929040690AG36GENIChomozygous116539050
102904060829040609AG39GENIChomozygous116539048
102904136729041368TC51GENIChomozygous116539052
102904156529041566GA27GENIChomozygous116539054
102904179929041800GT55GENICpossibly homozygous116539056
102904224229042243AG37GENIChomozygous116539058
102904246629042467CA45GENIChomozygous116539060
102904295029042951GT57GENIChomozygous116539062
102904301129043012AT58GENIChomozygous116750941
102904306929043070AT60GENIChomozygous116750947
102904428129044282CT48GENIChomozygous116539064