chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730625723062573TC24GENIChomozygous115546561
730626723062673CT48GENIChomozygous115546563
730640723064073GA31GENICheterozygous116401260
730668523066853AG55GENICheterozygous115546565
730670903067091CA25GENIChomozygous115546567
730671583067159CT28GENIChomozygous115546569
730672773067278GA31GENIChomozygous115546571
730673013067302GA35GENIChomozygous115546573
730689453068946GC23GENIChomozygous115546575
730707343070735TC28GENIChomozygous115546579
730715753071576AT14GENIChomozygous115546581
730720813072082CT16GENIChomozygous115546583
730727493072750TG26GENIChomozygous115546585
730742343074235CT33GENIChomozygous115546587
730779933077994AG15GENIChomozygous115546589
730791163079117CT33GENIChomozygous115546591
730805293080530TC28GENICheterozygous116401261
730807113080712TC32GENICheterozygous115977493
730830063083007AG11GENIChomozygous115546597
730812143081215CT32GENIChomozygous115546593
730827833082784TC23GENIChomozygous115546595
730835863083587TC10GENIChomozygous115546599
730838843083885AG27GENIChomozygous115546601
730847203084721TG37GENIChomozygous115546603
730852253085226CT13GENICheterozygous115546605
730872163087217AG34GENIChomozygous115546607
730874003087401AG34GENICpossibly homozygous115546609
730880313088032GA26GENICheterozygous116382772
730880473088048CA35GENICheterozygous116382773
730880593088060GA35GENICheterozygous116382774
730885803088581GA27GENIChomozygous115546611
730902353090236TC21GENIChomozygous115546613
730913203091321TC37GENIChomozygous115546615
730921453092146CT14GENIChomozygous115546617
730974923097493TG21GENIChomozygous115546619