chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105220979752209798GGGGGAGATAGAGAGAGGGGAGAGGGAGA3GENICheterozygous52460144
105221171352211714GGATCT3GENIChomozygous51454241
105221688352216885AC--6GENICheterozygous52376289
105222849952228500CCT7GENICheterozygous52800507
105222851852228519GT13GENIChomozygous51454276
105222889652228897CCTGTA2GENICheterozygous52318598
105228474652284747TA16GENIChomozygous51645643
105228614552286146GT37GENIChomozygous51882217
105228656052286561CT31GENIChomozygous51882220
105228679052286791TA32GENIChomozygous51454344
105228926352289264TC25GENIChomozygous51454346
105229085452290855CA52GENIChomozygous51882223
105229291352292914AT16GENIChomozygous51882226
105229656652296567AC16GENIChomozygous51454380
105229821752298220TTT---14GENICheterozygous51645648
105229821952298220T-14GENICpossibly homozygous51454391
105229825552298256GA27GENIChomozygous51882229
105229913252299133AG23GENIChomozygous51882232
105229996152299962G-34GENIChomozygous51645649
105230029652300297AT29GENIChomozygous51645650
105230036352300364CT23GENIChomozygous51645651
105230057152300572AG24GENIChomozygous51645652
105230110952301110GGA20GENIChomozygous51454397
105230157352301574GA27GENIChomozygous51454399
105225620152256203AG--9GENICheterozygous52723536