chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18402027402028TG21GENIChomozygous125342419
18402043402044AG14GENIChomozygous125342420
18402068402069TC18GENIChomozygous125342421
18402200402201CT16GENIChomozygous125342422
18402296402297GC7GENIChomozygous125342423
18402398402399GA15GENIChomozygous125342424
18403404403405TC18GENIChomozygous125342425
18403429403430GA9GENIChomozygous125342426
18404473404474AC24GENIChomozygous125342427
18404596404597AG15GENIChomozygous125342428
18404633404634CG13GENIChomozygous125342429
18405341405342TC3GENICheterozygous125342430
18405615405616CT19GENIChomozygous125342431
18405673405674GA10GENIChomozygous125342432
18405681405682TC14GENIChomozygous125342433
18405867405868TC16GENIChomozygous125342434
18406104406105AT20GENIChomozygous125342435
18406134406135AG20GENIChomozygous125342436
18406182406183GA7GENIChomozygous125342437
18406726406727TC6GENIChomozygous125342438
18406823406824TG19GENIChomozygous125342439
18406826406827CT20GENICheterozygous125342440
18407012407013TC20GENIChomozygous125342441
18407076407077GC15GENIChomozygous125342442
18407226407227AG14GENICheterozygous125342443