chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214824820214824821CA14GENIChomozygous108533039
1214825471214825472TC13GENIChomozygous108533040
1214825888214825889AC16GENIChomozygous109191930
1214827165214827166AG18GENIChomozygous108533042
1214827277214827278AT15GENIChomozygous109191932
1214827725214827726TA9GENIChomozygous109191934
1214828057214828058CT18GENICheterozygous109191936
1214828549214828550TC9GENIChomozygous109191938
1214829865214829866GA16GENIChomozygous108533045
1214830284214830285CT9GENIChomozygous108533046
1214832193214832194AT14GENIChomozygous108533047
1214832245214832246TC21GENIChomozygous108533048
1214832731214832732AG19GENIChomozygous108533049
1214834487214834488CT14GENIChomozygous108533050
1214834508214834509TC19GENIChomozygous109191940
1214836500214836501TC6GENIChomozygous108533051
1214836895214836896GA10GENIChomozygous108533052
1214836898214836899AG10GENIChomozygous108533053
1214836999214837000CG8GENIChomozygous108533054
1214837618214837619TC12GENIChomozygous108533056
1214839729214839730GA16GENIChomozygous109191942
1214828058214828059TC11GENICheterozygous125378262
1214828087214828088CG12GENICheterozygous125378263