chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1279798736279798737AC22GENIChomozygous108665360
1279798829279798830TA14GENIChomozygous108665362
1279798879279798880GC12GENIChomozygous108665363
1279799550279799551AG17GENIChomozygous108665365
1279802620279802621TC15GENIChomozygous108665367
1279804743279804744TC14GENIChomozygous108665368
1279805061279805062GT20GENICpossibly homozygous108665370
1279805357279805358AG17GENIChomozygous108665371
1279805505279805506GA11GENIChomozygous108665373
1279805688279805689TC17GENIChomozygous108665375
1279806098279806099CT7GENIChomozygous108665378
1279806466279806467CT22GENIChomozygous108665380
1279806861279806862CA29GENIChomozygous108665382
1279808362279808363GA27GENIChomozygous108665383
1279808515279808516GA31GENIChomozygous108665385
1279809011279809012AC22GENIChomozygous108665386
1279809824279809825CT25GENIChomozygous108665388
1279810130279810131GA25GENIChomozygous108665389
1279810161279810162AG31GENIChomozygous108665391
1279810520279810521CT27GENIChomozygous108665393
1279810534279810535AG27GENIChomozygous108665394
1279810759279810760TC29GENIChomozygous108665395
1279810760279810761AG29GENIChomozygous108665397
1279810834279810835AG25GENIChomozygous108665399
1279810994279810995AG23GENIChomozygous108665401
1279811025279811026TC27GENIChomozygous108665402
1279811077279811078AG28GENIChomozygous108665404
1279811170279811171AG20GENIChomozygous108665405
1279811196279811197CA19GENIChomozygous108665407
1279811205279811206TC22GENIChomozygous108665409