chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105220979752209798GGGGGAGATAGAGAGAGGGGAGAGGGAGA2GENIChomozygous52460144
105221171352211714GGATCT9GENIChomozygous51454241
105221688352216885AC--3GENICheterozygous52376289
105222849952228500CCT9GENICheterozygous52800507
105222851852228519GT13GENIChomozygous51454276
105225786952257871AG--9GENICheterozygous52460147
105227622752276228TTATC13GENIChomozygous51454327
105227767952277681GT--6GENICheterozygous51454329
105228194452281945TTATAC15GENIChomozygous52156381
105228474652284747TA23GENIChomozygous51645643
105228614552286146GT13GENIChomozygous51882217
105228656052286561CT36GENIChomozygous51882220
105228679052286791TA26GENIChomozygous51454344
105228926352289264TC21GENIChomozygous51454346
105229071752290735CTCTCTCTCTCTCTCACA------------------11GENICheterozygous52723543
105229085452290855CA22GENIChomozygous51882223
105229291352292914AT20GENIChomozygous51882226
105229656652296567AC17GENIChomozygous51454380
105229821852298220TT--21GENICheterozygous51454390
105229821952298220T-21GENICpossibly homozygous51454391
105229825552298256GA24GENIChomozygous51882229
105229913252299133AG19GENIChomozygous51882232
105229996152299962G-17GENIChomozygous51645649
105230029652300297AT12GENIChomozygous51645650
105230036352300364CT5GENIChomozygous51645651
105230057152300572AG18GENIChomozygous51645652
105230110952301110GGA27GENIChomozygous51454397
105230157352301574GA17GENIChomozygous51454399