chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91263442512634426AG55GENIChomozygous781180444
91263482512634826GT76GENICheterozygous781180445
91263513412635135AG87GENICheterozygous781180446
91263515712635158AG136GENICheterozygous781180447
91263517912635180AT164GENICheterozygous781180448
91263519012635191TC172GENICheterozygous781180449
91263553612635537TC102GENICheterozygous781180450
91263555912635560CG99GENICheterozygous781180451
91263590312635904CA113GENICheterozygous781180452
91263595812635959AG92GENICheterozygous781180453
91263603612636037CT89GENICheterozygous781180454
91263604212636043TC90GENICheterozygous781180455
91263605312636054AG87GENICheterozygous781180456
91263642412636425CT60GENICpossibly homozygous781180457
91263682812636829CA94GENICheterozygous781180458
91263685612636857GA101GENICheterozygous781180459
91263687912636880AC98GENICheterozygous781180460
91263744412637445AT86GENICpossibly homozygous781180461
91263786612637867AG148GENICheterozygous781180462
91263787212637873TG146GENICheterozygous781180463
91263789412637895AG148GENICheterozygous781180464
91263790412637905CG142GENICheterozygous781180465
91263791812637919AC136GENICheterozygous781180466
91263794612637947GA102GENICheterozygous781180467
91263932112639322TA70GENICpossibly homozygous781180468
91264020712640208TC84GENIChomozygous781180469
91264286912642870GC70GENIChomozygous781180470
91264365812643659CA71GENIChomozygous781180471
91264372212643723CA61GENICpossibly homozygous781180472
91264571112645712GA48GENIChomozygous781180473
91264721612647217AT47GENIChomozygous781180474
91264824512648246AG50GENIChomozygous781180475
91264826112648262GA42GENICpossibly homozygous781180476
91264942812649429TC78GENIChomozygous781180477
91265099512650996TC66GENIChomozygous781180478