chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA7GENIChomozygous71276356
4161446855161446856CG19GENIChomozygous71276358
4161446863161446864CT19GENIChomozygous71276360
4161448461161448462CT18GENIChomozygous71276362
4161448698161448699TC5GENICheterozygous71276366
4161449928161449929CT36GENIChomozygous71276388
4161450430161450431TC13GENIChomozygous71276390
4161450642161450643AC14GENIChomozygous71276392
4161450915161450916AG25GENIChomozygous71276394
4161451267161451268CT20GENIChomozygous71276396
4161451824161451825AG23GENIChomozygous71276398
4161452668161452669CT20GENIChomozygous71276400
4161452791161452792TC28GENIChomozygous71276402
4161453638161453639TC33GENIChomozygous71276404
4161453675161453676CT38GENIChomozygous71276406
4161454044161454045AG19GENIChomozygous71276408
4161454108161454109TC17GENIChomozygous71276410
4161454481161454482TC19GENIChomozygous71276412
4161454956161454957GA32GENIChomozygous71276413
4161455267161455268GA22GENIChomozygous71276415
4161455883161455884TC11GENIChomozygous71276417
4161456037161456038CG29GENICheterozygous71276425
4161456045161456046CG34GENICheterozygous71276427
4161456782161456783GA18GENIChomozygous71276429
4161457019161457020GA21GENIChomozygous71276431
4161457528161457529CT28GENIChomozygous71276433
4161459693161459694CT23GENIChomozygous71276435
4161460513161460514TC15GENIChomozygous71276437
4161460619161460620CT32GENIChomozygous71276439
4161463155161463156TG29GENIChomozygous71276441
4161463525161463526AG26GENIChomozygous71276443