chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249514211249515AG26GENIChomozygous992720353
1211249867211249868GA26GENIChomozygous992720354
1211249879211249880GT29GENIChomozygous992720355
1211250193211250194AC24GENIChomozygous992720356
1211250496211250497TC17GENIChomozygous992720357
1211250622211250623CG29GENIChomozygous992720358
1211250623211250624CT29GENIChomozygous992720359
1211250700211250701GA26GENIChomozygous992720360
1211252203211252204AG29GENIChomozygous992720361
1211252677211252678CT32GENIChomozygous992720362
1211254276211254277AC25GENIChomozygous992720363
1211254477211254478TC28GENIChomozygous992720364
1211254496211254497CT28GENIChomozygous992720365
1211255440211255441GT30GENICpossibly homozygous992720366
1211255616211255617AT30GENIChomozygous992720367
1211256722211256723TC16GENIChomozygous992720368
1211257074211257075AG24GENIChomozygous992720369
1211258234211258235GA41GENIChomozygous992720370
1211258541211258542CT32GENIChomozygous992720371
1211258803211258804TC28GENIChomozygous992720372
1211259737211259738AG28GENIChomozygous992720373
1211259868211259869CT35GENIChomozygous992720374
1211260475211260476CG27GENIChomozygous992720375
1211261011211261012GA44GENIChomozygous992720376
1211261278211261279AG24GENIChomozygous992720377
1211261430211261431CT28GENIChomozygous992720378
1211261727211261728CT19GENIChomozygous992720379
1211262253211262254CT39GENIChomozygous992720380
1211262513211262514GA35GENIChomozygous992720381
1211262865211262866AG27GENIChomozygous992720382
1211263517211263518CA22GENIChomozygous992720383
1211264098211264099TG28GENIChomozygous992720384
1211264888211264889CA31GENIChomozygous992720385
1211264889211264890TA30GENIChomozygous992720386