chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5167672374167672375GA8GENIChomozygous119206702
5167673011167673012CT17GENIChomozygous114455428
5167673282167673283TA19GENIChomozygous114455429
5167673658167673659CT4GENIChomozygous119206703
5167673840167673841CT17GENIChomozygous119206704
5167677103167677104CA17GENIChomozygous114455432
5167677146167677147TC9GENIChomozygous114455433
5167677227167677228GA12GENIChomozygous114455434
5167677396167677397GA20GENIChomozygous114455435
5167677563167677564AG8GENIChomozygous114455436
5167678037167678038CT5GENICheterozygous119258864
5167680259167680260AT13GENIChomozygous118987301
5167680767167680768CT6GENIChomozygous119206705
5167681779167681780CT19GENIChomozygous119206706
5167682489167682490CT6GENICheterozygous114082557
5167682789167682790AT12GENIChomozygous114082559
5167684441167684442CT10GENIChomozygous119206707
5167686062167686063TC11GENIChomozygous114082571
5167687196167687197TC17GENIChomozygous114082573
5167687572167687573GA13GENIChomozygous119206708
5167687866167687867TC10GENIChomozygous119206709
5167678350167678351TG4GENIChomozygous126315658
5167678792167678793TC8GENIChomozygous126315659
5167683069167683070GA8GENIChomozygous126315660
5167685564167685565GC13GENICheterozygous126315661
5167691220167691221AC7GENIChomozygous119206710
5167692137167692138GT4GENIChomozygous118987315
5167691253167691254AC9GENIChomozygous119206711
5167691263167691264CA11GENICheterozygous119206712
5167691835167691836CT12GENIChomozygous119258865
5167692472167692473TC17GENICpossibly homozygous114082590
5167692617167692618GA15GENIChomozygous119206713
5167695797167695798AT4GENIChomozygous114082608
5167695789167695790AG5GENIChomozygous126207416