chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151105715151105716AG17GENICpossibly homozygous111776249
3151105843151105844CT17GENIChomozygous112041417
3151106871151106872AT12GENIChomozygous111776257
3151110612151110613GC16GENIChomozygous112041419
3151111952151111953GA20GENIChomozygous111776285
3151112839151112840AG12GENIChomozygous112041423
3151113648151113649GA21GENIChomozygous112041425
3151115393151115394CT11GENIChomozygous111776291
3151116321151116322GA15GENIChomozygous112041429
3151117846151117847GA8GENIChomozygous111776303
3151118387151118388CT26GENIChomozygous112041431
3151119086151119087GC14GENICpossibly homozygous111776305
3151123892151123893TC12GENIChomozygous111776307
3151125409151125410TA16GENIChomozygous112041437
3151125519151125520AT16GENIChomozygous111776317
3151126450151126451GA11GENIChomozygous112041439
3151128900151128901AG6GENIChomozygous111776321
3151128922151128923AG5GENIChomozygous111776323
3151129013151129014TC9GENIChomozygous111776325
3151129695151129696AG12GENIChomozygous111776327
3151129767151129768TG12GENIChomozygous119830358
3151129769151129770TG13GENIChomozygous112041443
3151131649151131650AG20GENIChomozygous111776335
3151132425151132426CG11GENIChomozygous112041445
3151132436151132437GA9GENIChomozygous112041447
3151133437151133438TC10GENIChomozygous111776337
3151133593151133594TC13GENIChomozygous111776339
3151134482151134483AG10GENIChomozygous111776345
3151134889151134890CT6GENIChomozygous111776347
3151135532151135533CG14GENIChomozygous111776349
3151136234151136235AG6GENIChomozygous111776351
3151139853151139854GA11GENIChomozygous112041455
3151141940151141941GA12GENIChomozygous111776359
3151142105151142106AG11GENIChomozygous112041457
3151142311151142312CG10GENIChomozygous111776361
3151143197151143198AG15GENIChomozygous111776363
3151145317151145318AG10GENIChomozygous111776367
3151147812151147813GA5GENIChomozygous112041459
3151150390151150391AG17GENIChomozygous111776377