chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1270950943270950944CT20GENICpossibly homozygous61216303
1270951026270951027AACAGACACATGGTAGGTGAGCACAGGTAAT1GENIChomozygous62112387
1270951406270951407AG3GENIChomozygous61216323
1270951475270951476CA23GENICpossibly homozygous61216325
1270951876270951877TA23GENIChomozygous61216329
1270951901270951902TC21GENIChomozygous61216331
1270952028270952029CT18GENIChomozygous62112388
1270952088270952089TC9GENICpossibly homozygous61216335
1270952481270952482GA21GENICpossibly homozygous62112389
1270952757270952758AG18GENIChomozygous61216337
1270952795270952796AG22GENIChomozygous61216339
1270953055270953056CT22GENICpossibly homozygous61216341
1270953424270953425GA23GENIChomozygous62112390
1270953615270953616TC14GENICpossibly homozygous61216349
1270954226270954227AG15GENICpossibly homozygous61216351
1270954477270954478CA16GENIChomozygous61216353
1270954921270954922TC18GENICpossibly homozygous61216359
1270954993270954994TC15GENIChomozygous61216361
1270955550270955554GGCT----9GENIChomozygous61216367