chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15779421257794213TG33GENIChomozygous936982487
15779574457795745TC20GENIChomozygous936982488
15779591657795917CT17GENIChomozygous936982489
15779770657797707AG23GENIChomozygous936982490
15779934557799346CT29GENIChomozygous936982491
15779989457799895GA18GENIChomozygous936982492
15780045857800459TC26GENIChomozygous936982493
15780096457800965GA21GENIChomozygous936982494
15780102657801027CT28GENIChomozygous936982495
15780128157801282GA22GENIChomozygous936982496
15780273957802740GC14GENIChomozygous936982497
15780296957802970TC23GENIChomozygous936982498
15780299057802991CT26GENIChomozygous936982499
15780344257803443TA21GENIChomozygous936982500
15780356157803562TA20GENIChomozygous936982501
15780813357808134AG14GENIChomozygous936982502
15780824057808241TA21GENIChomozygous936982503
15780833457808335TC22GENIChomozygous936982504
15780839757808398TC17GENIChomozygous936982505
15780866357808664AG23GENIChomozygous936982506
15780868657808687GA22GENIChomozygous936982507
15780884057808841AG32GENIChomozygous936982508
15780898457808985AG29GENIChomozygous936982509
15780899457808995GA30GENIChomozygous936982510
15781073657810737GA28GENIChomozygous936982511
15781326557813266AT41GENIChomozygous936982512
15781551557815516AC9GENIChomozygous936982513
15781552957815530CT10GENIChomozygous936982514
15781649857816499CG23GENIChomozygous936982515
15781678257816783CT36GENIChomozygous936982516
15781701057817011TA28GENIChomozygous936982517
15781766557817666TC25GENIChomozygous936982518
15781851957818520AG15GENIChomozygous936982519
15781900157819002CT19GENIChomozygous936982520
15781903257819033CA16GENIChomozygous936982521