chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA24GENIChomozygous71276356
4161446855161446856CG37GENIChomozygous71276358
4161446863161446864CT35GENIChomozygous71276360
4161448461161448462CT24GENIChomozygous71276362
4161448698161448699TC31GENICheterozygous71276366
4161449928161449929CT35GENIChomozygous71276388
4161450430161450431TC24GENIChomozygous71276390
4161450642161450643AC34GENIChomozygous71276392
4161450915161450916AG32GENIChomozygous71276394
4161451267161451268CT15GENIChomozygous71276396
4161451824161451825AG34GENIChomozygous71276398
4161452668161452669CT46GENIChomozygous71276400
4161452791161452792TC35GENIChomozygous71276402
4161453638161453639TC21GENIChomozygous71276404
4161453675161453676CT28GENIChomozygous71276406
4161454044161454045AG14GENIChomozygous71276408
4161454108161454109TC14GENIChomozygous71276410
4161454481161454482TC25GENIChomozygous71276412
4161454956161454957GA24GENIChomozygous71276413
4161455267161455268GA32GENIChomozygous71276415
4161455883161455884TC13GENIChomozygous71276417
4161456037161456038CG52GENICheterozygous71276425
4161456045161456046CG55GENICheterozygous71276427
4161456782161456783GA37GENIChomozygous71276429
4161457019161457020GA45GENIChomozygous71276431
4161457528161457529CT34GENIChomozygous71276433
4161459693161459694CT35GENIChomozygous71276435
4161460513161460514TC21GENIChomozygous71276437
4161460619161460620CT38GENIChomozygous71276439
4161463155161463156TG24GENIChomozygous71276441
4161463525161463526AG25GENIChomozygous71276443