chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA15GENIChomozygous71276356
4161446855161446856CG16GENICpossibly homozygous71276358
4161446863161446864CT16GENIChomozygous71276360
4161448461161448462CT11GENIChomozygous71276362
4161449928161449929CT20GENICpossibly homozygous71276388
4161450430161450431TC14GENIChomozygous71276390
4161450642161450643AC19GENIChomozygous71276392
4161450915161450916AG23GENIChomozygous71276394
4161451267161451268CT16GENICpossibly homozygous71276396
4161451824161451825AG19GENIChomozygous71276398
4161452668161452669CT27GENIChomozygous71276400
4161452791161452792TC26GENIChomozygous71276402
4161453638161453639TC29GENIChomozygous71276404
4161453675161453676CT22GENIChomozygous71276406
4161454044161454045AG19GENIChomozygous71276408
4161454108161454109TC26GENIChomozygous71276410
4161454481161454482TC11GENIChomozygous71276412
4161454956161454957GA17GENIChomozygous71276413
4161455267161455268GA20GENIChomozygous71276415
4161455883161455884TC9GENIChomozygous71276417
4161456037161456038CG25GENICheterozygous71276425
4161456045161456046CG26GENICheterozygous71276427
4161456782161456783GA22GENICpossibly homozygous71276429
4161457019161457020GA24GENIChomozygous71276431
4161457528161457529CT23GENIChomozygous71276433
4161459693161459694CT15GENIChomozygous71276435
4161460513161460514TC20GENICpossibly homozygous71276437
4161460619161460620CT15GENIChomozygous71276439
4161463155161463156TG16GENIChomozygous71276441
4161463525161463526AG22GENIChomozygous71276443