chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185503095455030955GT56GENICpossibly homozygous63895766
185503099255030993AG52GENICpossibly homozygous63895767
185503493355034934AG35GENIChomozygous63895768
185503657555036576AT58GENIChomozygous63895769
185503807655038077GA55GENIChomozygous63895770
185503830755038308TG47GENIChomozygous63895771
185503873455038735AG27GENIChomozygous63895772
185503893955038940AG40GENIChomozygous63895773
185503992055039921AG22GENIChomozygous63895774
185504375355043754AT43GENICpossibly homozygous63895777
185504390555043906AC36GENIChomozygous63895778
185504405055044051AG48GENIChomozygous63895779
185504424655044247CT52GENIChomozygous63895780
185504549555045496TC24GENIChomozygous63895781
185504654255046543TC13GENIChomozygous63895782
185504667255046673TC21GENIChomozygous63895783
185504923955049240AG59GENIChomozygous63895784
185504978055049781CG51GENIChomozygous63895785
185504988655049887GA53GENIChomozygous63895786
185505021055050211CG28GENIChomozygous63895787
185505118055051181AG10GENIChomozygous63895790
185505047155050472AC30GENIChomozygous63895788
185505088155050882TG26GENIChomozygous63895789
185505230155052302CT36GENIChomozygous63895791
185505244355052444AG28GENIChomozygous63895792