chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122559737225597373AG21GENIChomozygous50141615
122559890925598910GGGA14GENICheterozygous50372063
122559891025598912GA--14GENICpossibly homozygous50141617
122559942625599427TTA12GENIChomozygous50296506
122560009825600099GGA4GENIChomozygous50296508
122560011625600117CCA8GENIChomozygous50404070
122560275525602756GGCA6GENICheterozygous50141623
122560275825602760CA--6GENICheterozygous50141625
122560307625603077TC26GENIChomozygous50296512
122560413925604140A-2GENIChomozygous50141630
122560532425605325AG30GENIChomozygous50296516
122560597425605975GGA31GENICpossibly homozygous50404072
122560722325607224CT23GENIChomozygous50296518
122561045125610452GT34GENIChomozygous50404074
122561133725611338T-23GENIChomozygous50141656
122561363825613639TTAAA7GENIChomozygous50296528
122561429325614294TA32GENICpossibly homozygous50404076
122561471225614713CA38GENIChomozygous50141721
122561767525617679AAAA----8GENIChomozygous50296534
122561798425617985CT21GENIChomozygous50404078
122561869825618699AAG13GENICheterozygous50141789
122561869925618700AG14GENICheterozygous50372065
122562086225620863AG26GENIChomozygous50141797
122562092925620934AAACA-----23GENIChomozygous50141800
122562093325620934A-21GENIChomozygous50141802
122562103925621040TC26GENIChomozygous50141804
122562120125621202GGT5GENICheterozygous50404080
122562120325621205TT--5GENICheterozygous50141808
122562136825621369C-19GENIChomozygous50141810
122562137725621378CCA21GENICheterozygous50404082
122562148625621487GC28GENICpossibly homozygous50296546
122562207325622074TC31GENIChomozygous50141816
122562216525622166GA33GENIChomozygous50296550
122562278425622785AAGGG10GENIChomozygous50141818
122562398525623986GA19GENIChomozygous50404084