chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1279798463279798463T44GENIChomozygous127517616
1279798736279798737AC39GENIChomozygous108665360
1279798829279798830TA51GENIChomozygous108665362
1279798879279798880GC55GENIChomozygous108665363
1279799550279799551AG42GENIChomozygous108665365
1279802620279802621TC50GENIChomozygous108665367
1279804743279804744TC54GENIChomozygous108665368
1279799793279799794CT57GENIChomozygous109035069
1279801151279801152TC33GENIChomozygous109035070
1279802596279802597CT40GENIChomozygous109035071
1279805227279805228GT45GENIChomozygous109035073
1279805357279805358AG49GENIChomozygous108665371
1279805443279805444GA49GENIChomozygous109035074
1279806475279806476CT41GENIChomozygous109035076
1279806759279806760A42GENIChomozygous127517619
1279806861279806862CA48GENIChomozygous108665382
1279808362279808363GA45GENIChomozygous108665383
1279809011279809012AC45GENIChomozygous108665386
1279809824279809825CT50GENIChomozygous108665388
1279810130279810131GA42GENIChomozygous108665389
1279810161279810162AG41GENIChomozygous108665391
1279810363279810377CAAGTTTCATATAG57GENIChomozygous127517620
1279810520279810521CT45GENIChomozygous108665393
1279810534279810535AG42GENIChomozygous108665394
1279810759279810760TC54GENIChomozygous108665395
1279810760279810761AG54GENIChomozygous108665397
1279810834279810835AG55GENIChomozygous108665399
1279810959279810960CT39GENIChomozygous109035077
1279810994279810995AG44GENIChomozygous108665401
1279811025279811026TC48GENIChomozygous108665402
1279811077279811078AG50GENIChomozygous108665404
1279811170279811171AG36GENIChomozygous108665405
1279805915279805943TGTGTGTCCAGGCCATCCAGGAGATGTG36GENIChomozygous131269640
1279811196279811197CA36GENIChomozygous108665407
1279811205279811206TC36GENIChomozygous108665409