chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106141456061414561GT3GENIChomozygous116790509
106141456161414562AT3GENIChomozygous116612767
106141464161414642AG18GENIChomozygous118067733
106141489361414894GT29GENIChomozygous116612769
106141538061415381TG14GENIChomozygous116612771
106141495761414958AG28GENIChomozygous116939349
106141508161415082CT21GENIChomozygous116939351
106141570561415706TC19GENIChomozygous116939353
106141614861416149CT32GENIChomozygous116939357
106141615261416153AG31GENIChomozygous116939359
106141620261416203TG26GENIChomozygous116790521
106141727961417280GT17GENIChomozygous116939361
106141838161418382AC14GENIChomozygous116612775
106141851361418514TC27GENIChomozygous116939363
106141882961418830GC35GENIChomozygous116939365
106141907661419077CT15GENIChomozygous116939367
106141908261419083CG13GENIChomozygous116939369
106141946561419466TG26GENIChomozygous116612779
106141953761419538CA32GENIChomozygous116790525
106141954861419549GC20GENIChomozygous116790527
106141954961419550GA20GENIChomozygous116939371
106141963661419637GA39GENIChomozygous117079862
106141987961419880CG24GENIChomozygous116612783
106141992061419921CA25GENIChomozygous116612785
106142010361420104TG14GENIChomozygous117997182
106142044961420450GA25GENIChomozygous116612787
106142190561421906CT26GENIChomozygous116939375