chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG36GENIChomozygous962994399
1211250496211250497TC27GENIChomozygous962994400
1211250622211250623CG28GENIChomozygous962994401
1211250971211250972AC40GENIChomozygous962994402
1211251987211251988GA40GENIChomozygous962994403
1211252068211252069CT39GENIChomozygous962994404
1211252076211252077AC33GENIChomozygous962994405
1211252203211252204AG20GENIChomozygous962994406
1211254118211254119AT36GENIChomozygous962994407
1211254143211254144CT38GENIChomozygous962994408
1211254145211254146CT39GENIChomozygous962994409
1211254496211254497CT28GENIChomozygous962994410
1211254854211254855CG35GENIChomozygous962994411
1211255440211255441GT27GENIChomozygous962994412
1211255616211255617AT38GENIChomozygous962994413
1211256722211256723TC31GENIChomozygous962994414
1211257074211257075AG30GENIChomozygous962994415
1211257451211257452CT39GENIChomozygous962994416
1211258803211258804TC30GENIChomozygous962994417
1211259737211259738AG21GENIChomozygous962994418
1211260475211260476CG45GENIChomozygous962994419
1211261278211261279AG33GENIChomozygous962994420
1211261430211261431CT35GENIChomozygous962994421
1211262513211262514GA44GENIChomozygous962994422
1211262865211262866AG40GENIChomozygous962994423
1211264098211264099TG34GENIChomozygous962994424