chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161446528161446529GA11GENIChomozygous71276356
4161446855161446856CG15GENIChomozygous71276358
4161446863161446864CT19GENIChomozygous71276360
4161448461161448462CT14GENICpossibly homozygous71276362
4161449928161449929CT25GENIChomozygous71276388
4161450430161450431TC18GENIChomozygous71276390
4161452791161452792TC33GENIChomozygous71276402
4161450642161450643AC20GENIChomozygous71276392
4161450915161450916AG17GENIChomozygous71276394
4161451267161451268CT13GENIChomozygous71276396
4161451824161451825AG23GENIChomozygous71276398
4161452668161452669CT18GENIChomozygous71276400
4161453638161453639TC18GENIChomozygous71276404
4161453675161453676CT21GENIChomozygous71276406
4161454044161454045AG18GENIChomozygous71276408
4161454108161454109TC17GENIChomozygous71276410
4161454481161454482TC14GENICpossibly homozygous71276412
4161454956161454957GA20GENIChomozygous71276413
4161455267161455268GA26GENIChomozygous71276415
4161455883161455884TC6GENIChomozygous71276417
4161456037161456038CG12GENICheterozygous71276425
4161456045161456046CG11GENICheterozygous71276427
4161456782161456783GA11GENIChomozygous71276429
4161457019161457020GA23GENIChomozygous71276431
4161457528161457529CT24GENIChomozygous71276433
4161459693161459694CT22GENIChomozygous71276435
4161460513161460514TC10GENIChomozygous71276437
4161460619161460620CT30GENIChomozygous71276439
4161463155161463156TG15GENIChomozygous71276441
4161463525161463526AG26GENIChomozygous71276443