chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1279798736279798737AC24GENIChomozygous108665360
1279798829279798830TA26GENIChomozygous108665362
1279798879279798880GC29GENIChomozygous108665363
1279799550279799551AG25GENIChomozygous108665365
1279799793279799794CT34GENIChomozygous109035069
1279801151279801152TC22GENIChomozygous109035070
1279802512279802513GA21GENIChomozygous120496393
1279802596279802597CT27GENIChomozygous109035071
1279802620279802621TC29GENIChomozygous108665367
1279804743279804744TC38GENIChomozygous108665368
1279805061279805062GA30GENIChomozygous109035072
1279805227279805228GT17GENIChomozygous109035073
1279805357279805358AG16GENIChomozygous108665371
1279805443279805444GA16GENIChomozygous109035074
1279806475279806476CT24GENIChomozygous109035076
1279806861279806862CA24GENIChomozygous108665382
1279808362279808363GA26GENIChomozygous108665383
1279809011279809012AC32GENIChomozygous108665386
1279809824279809825CT15GENIChomozygous108665388
1279810130279810131GA15GENIChomozygous108665389
1279810161279810162AG15GENIChomozygous108665391
1279810520279810521CT20GENIChomozygous108665393
1279810534279810535AG20GENIChomozygous108665394
1279810759279810760TC24GENIChomozygous108665395
1279810760279810761AG26GENICpossibly homozygous108665397
1279810834279810835AG18GENIChomozygous108665399
1279810959279810960CT28GENIChomozygous109035077
1279810994279810995AG26GENIChomozygous108665401
1279811025279811026TC34GENIChomozygous108665402
1279811077279811078AG27GENIChomozygous108665404
1279811170279811171AG27GENIChomozygous108665405
1279811196279811197CA30GENIChomozygous108665407
1279811205279811206TC28GENIChomozygous108665409