chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA24GENIChomozygous71276356
4161446855161446856CG31GENIChomozygous71276358
4161446863161446864CT34GENIChomozygous71276360
4161448461161448462CT24GENIChomozygous71276362
4161448673161448674CA20GENICheterozygous71276364
4161448716161448717TC11GENICheterozygous71276368
4161448737161448738TC12GENICheterozygous71662204
4161448767161448768TC18GENICheterozygous71276372
4161449928161449929CT29GENIChomozygous71276388
4161450430161450431TC33GENIChomozygous71276390
4161450642161450643AC36GENIChomozygous71276392
4161450915161450916AG32GENIChomozygous71276394
4161451267161451268CT44GENIChomozygous71276396
4161451824161451825AG48GENIChomozygous71276398
4161452668161452669CT33GENIChomozygous71276400
4161452791161452792TC27GENIChomozygous71276402
4161453638161453639TC42GENIChomozygous71276404
4161453675161453676CT46GENIChomozygous71276406
4161454044161454045AG50GENIChomozygous71276408
4161454108161454109TC43GENIChomozygous71276410
4161454481161454482TC35GENIChomozygous71276412
4161454956161454957GA37GENIChomozygous71276413
4161455267161455268GA27GENIChomozygous71276415
4161455883161455884TC24GENIChomozygous71276417
4161456021161456022CG16GENICheterozygous71276421
4161456025161456026CG17GENICheterozygous71276423
4161456037161456038CG19GENICheterozygous71276425
4161456045161456046CG23GENICheterozygous71276427
4161456782161456783GA39GENIChomozygous71276429
4161457019161457020GA43GENIChomozygous71276431
4161457528161457529CT48GENIChomozygous71276433
4161459693161459694CT38GENIChomozygous71276435
4161460513161460514TC19GENIChomozygous71276437
4161460619161460620CT38GENICpossibly homozygous71276439
4161463155161463156TG44GENIChomozygous71276441
4161463525161463526AG33GENIChomozygous71276443