chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA19GENIChomozygous71276356
4161446855161446856CG16GENIChomozygous71276358
4161446863161446864CT15GENIChomozygous71276360
4161448461161448462CT14GENICpossibly homozygous71276362
4161448698161448699TC48GENICheterozygous71276366
4161449928161449929CT19GENIChomozygous71276388
4161450430161450431TC26GENIChomozygous71276390
4161450642161450643AC24GENIChomozygous71276392
4161450915161450916AG22GENIChomozygous71276394
4161451267161451268CT17GENICpossibly homozygous71276396
4161451824161451825AG27GENIChomozygous71276398
4161452668161452669CT16GENIChomozygous71276400
4161452791161452792TC26GENIChomozygous71276402
4161453638161453639TC25GENIChomozygous71276404
4161453675161453676CT23GENIChomozygous71276406
4161454044161454045AG18GENIChomozygous71276408
4161454108161454109TC25GENIChomozygous71276410
4161454481161454482TC26GENIChomozygous71276412
4161454956161454957GA22GENIChomozygous71276413
4161455267161455268GA22GENIChomozygous71276415
4161455883161455884TC15GENIChomozygous71276417
4161456037161456038CG23GENICheterozygous71276425
4161456045161456046CG27GENICheterozygous71276427
4161456782161456783GA27GENIChomozygous71276429
4161457019161457020GA26GENIChomozygous71276431
4161457528161457529CT21GENIChomozygous71276433
4161459693161459694CT21GENIChomozygous71276435
4161460513161460514TC10GENIChomozygous71276437
4161460619161460620CT23GENIChomozygous71276439
4161463155161463156TG19GENIChomozygous71276441
4161463525161463526AG19GENIChomozygous71276443