chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141965019141965020GC4GENICheterozygous56188449
5141965611141965612AG10GENICpossibly homozygous56188450
5141967069141967070AG11GENICheterozygous56188451
5141971908141971909CG8GENICheterozygous55756360
5141972580141972581AG7GENICpossibly homozygous55756363
5141977160141977161TTTC6GENIChomozygous56066590
5141977212141977213TC13GENIChomozygous55910026
5141979107141979108TC2GENIChomozygous55756377
5141986064141986065AG8GENIChomozygous56188452
5141986843141986844GC9GENIChomozygous56188453
5141987003141987004GA5GENIChomozygous55910057
5141988122141988123CT3GENIChomozygous56188454
5141988339141988340TA9GENIChomozygous55756404
5141988495141988496AG5GENIChomozygous55756406
5141988959141988960CT6GENIChomozygous55756407
5141989012141989013AG5GENIChomozygous55756408
5141989178141989179AG10GENIChomozygous55756409
5141989415141989419TAGA----6GENIChomozygous55756410
5141990084141990085AT17GENICpossibly homozygous56188455
5141990292141990293AC12GENICpossibly homozygous55756412
5141990971141990972AG14GENICpossibly homozygous55756415
5141991144141991145CT13GENICpossibly homozygous55756416
5141991764141991765CT2GENIChomozygous56188456
5141991848141991849AC9GENIChomozygous55756419
5141992008141992009AAT4GENIChomozygous55910065
5141992523141992525AA--6GENIChomozygous56188457