chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107800592478005925TC18GENIChomozygous116642804
107800599278005993AG26GENIChomozygous116642806
107800637778006378TC35GENIChomozygous116642808
107800724578007246AG28GENIChomozygous116642810
107800731978007320AG24GENIChomozygous116642812
107800741678007417AG14GENIChomozygous116642814
107800757978007580TG26GENIChomozygous116642816
107800772278007723AG38GENIChomozygous116642818
107800833878008339GA24GENIChomozygous116642820
107800838878008389CT30GENIChomozygous116642822
107800895278008953TC26GENIChomozygous116642824
107800912378009124CG32GENIChomozygous116642826
107800913478009135CT33GENIChomozygous116642828
107800928878009289GA30GENIChomozygous116642830
107800963878009639CT13GENIChomozygous116642832
107800979978009800CT24GENIChomozygous116642834
107801072978010730GA24GENIChomozygous116642836
107801103678011037GA14GENIChomozygous116642838
107801154778011548CT32GENIChomozygous116642840
107801219178012192CA29GENIChomozygous116642842
107801230878012309AG24GENIChomozygous116642844
107801233278012333TA20GENIChomozygous116642846
107801256578012566CT34GENIChomozygous116642848
107801270878012709CT39GENIChomozygous116642850
107801287178012872CT35GENIChomozygous116642852
107801289678012897TC30GENIChomozygous116642854
107801327678013277GT31GENIChomozygous116642858
107801327978013280GA30GENIChomozygous116642860
107801336178013362GA24GENIChomozygous116642862
107801338878013389TG25GENIChomozygous116642864
107801347578013476AC27GENIChomozygous116642866
107801348078013481GA26GENIChomozygous116642868
107801590378015904GA12GENIChomozygous116642870
107801097078010971AT14GENIChomozygous117132498
107801271378012714CA41GENIChomozygous117132499
107802339978023400CG14GENIChomozygous117132503
107803315878033159CA24GENIChomozygous116642943
107813465378134654CT13GENIChomozygous116643217
107813467878134679CT16GENIChomozygous116643219
107815102578151026AT7GENIChomozygous117328612