chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA19GENIChomozygous71276356
4161446855161446856CG10GENIChomozygous71276358
4161448519161448520GA3GENIChomozygous73533364
4161449928161449929CT16GENICheterozygous71276388
4161450430161450431TC5GENIChomozygous71276390
4161450642161450643AC25GENIChomozygous71276392
4161450915161450916AG22GENIChomozygous71276394
4161451267161451268CT13GENIChomozygous71276396
4161451824161451825AG32GENIChomozygous71276398
4161452668161452669CT32GENIChomozygous71276400
4161452791161452792TC14GENIChomozygous71276402
4161453638161453639TC9GENIChomozygous71276404
4161453675161453676CT23GENIChomozygous71276406
4161454044161454045AG11GENIChomozygous71276408
4161454481161454482TC11GENIChomozygous71276412
4161454956161454957GA28GENIChomozygous71276413
4161456045161456046CG6GENIChomozygous71276427
4161455267161455268GA16GENIChomozygous71276415
4161455883161455884TC13GENIChomozygous71276417
4161456782161456783GA14GENIChomozygous71276429
4161457019161457020GA9GENIChomozygous71276431
4161457528161457529CT21GENIChomozygous71276433
4161459693161459694CT17GENIChomozygous71276435
4161460513161460514TC18GENICheterozygous71276437
4161460619161460620CT9GENIChomozygous71276439
4161463155161463156TG17GENIChomozygous71276441
4161463525161463526AG31GENIChomozygous71276443
4161464184161464185AG15GENICheterozygous72716120