chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA7GENIChomozygous71276356
4161446855161446856CG11GENIChomozygous71276358
4161446863161446864CT10GENIChomozygous71276360
4161448461161448462CT4GENIChomozygous71276362
4161449928161449929CT19GENIChomozygous71276388
4161450430161450431TC15GENIChomozygous71276390
4161450642161450643AC18GENIChomozygous71276392
4161450915161450916AG13GENIChomozygous71276394
4161451267161451268CT17GENIChomozygous71276396
4161451824161451825AG15GENIChomozygous71276398
4161452668161452669CT14GENIChomozygous71276400
4161452791161452792TC29GENIChomozygous71276402
4161453638161453639TC24GENIChomozygous71276404
4161453675161453676CT23GENICpossibly homozygous71276406
4161454044161454045AG16GENIChomozygous71276408
4161454108161454109TC11GENIChomozygous71276410
4161454481161454482TC11GENIChomozygous71276412
4161454956161454957GA18GENIChomozygous71276413
4161455267161455268GA29GENIChomozygous71276415
4161455883161455884TC1GENIChomozygous71276417
4161456037161456038CG13GENICheterozygous71276425
4161456045161456046CG12GENICheterozygous71276427
4161456782161456783GA17GENIChomozygous71276429
4161457019161457020GA18GENIChomozygous71276431
4161457528161457529CT24GENIChomozygous71276433
4161459693161459694CT20GENIChomozygous71276435
4161460513161460514TC16GENIChomozygous71276437
4161460619161460620CT17GENIChomozygous71276439
4161463155161463156TG18GENIChomozygous71276441
4161463525161463526AG14GENIChomozygous71276443