chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1279798736279798737AC19GENIChomozygous108665360
1279798829279798830TA18GENIChomozygous108665362
1279798879279798880GC17GENIChomozygous108665363
1279799550279799551AG11GENIChomozygous108665365
1279802620279802621TC19GENIChomozygous108665367
1279804743279804744TC10GENIChomozygous108665368
1279805061279805062GT17GENIChomozygous108665370
1279805357279805358AG11GENIChomozygous108665371
1279805505279805506GA5GENIChomozygous108665373
1279805688279805689TC11GENIChomozygous108665375
1279806098279806099CT13GENIChomozygous108665378
1279806466279806467CT27GENIChomozygous108665380
1279808362279808363GA24GENIChomozygous108665383
1279808515279808516GA17GENIChomozygous108665385
1279809011279809012AC16GENIChomozygous108665386
1279809824279809825CT14GENIChomozygous108665388
1279810130279810131GA16GENIChomozygous108665389
1279810161279810162AG17GENIChomozygous108665391
1279810520279810521CT15GENIChomozygous108665393
1279810534279810535AG11GENIChomozygous108665394
1279810834279810835AG21GENIChomozygous108665399
1279810994279810995AG13GENIChomozygous108665401
1279811025279811026TC14GENIChomozygous108665402
1279811077279811078AG18GENIChomozygous108665404
1279811170279811171AG21GENIChomozygous108665405
1279811196279811197CA16GENIChomozygous108665407
1279811205279811206TC19GENIChomozygous108665409