chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138380757083807571CT50GENIChomozygous777023544
138381126883811269TC54GENIChomozygous777023545
138381272483812725GA26GENICpossibly homozygous777023546
138381327283813273GA46GENIChomozygous777023547
138381452283814523CT64GENIChomozygous777023548
138381557483815575CA66GENIChomozygous777023549
138381692183816922TC58GENIChomozygous777023550
138381912283819123AT22GENIChomozygous777023551
138382161383821614GT49GENIChomozygous777023552
138382177683821777GC50GENIChomozygous777023553
138382471483824715GA44GENIChomozygous777023554
138382518483825185CT71GENIChomozygous777023555
138382678083826781GA45GENIChomozygous777023556
138382777383827774GA40GENIChomozygous777023557
138382781583827816CT37GENIChomozygous777023558
138382841683828417TG56GENIChomozygous777023559
138382857883828579TG41GENIChomozygous777023560
138383126983831270AG7GENIChomozygous777023561
138383127583831276AG5GENIChomozygous777023562
138383128183831282AG5GENIChomozygous777023563
138383129383831294AG6GENIChomozygous777023564
138383129983831300AG7GENIChomozygous777023565
138383130583831306AG9GENIChomozygous777023566
138383136683831367TC33GENICpossibly homozygous777023567
138383420883834209GA39GENIChomozygous777023568
138383433183834332AG56GENICpossibly homozygous777023569
138383514083835141AG42GENIChomozygous777023570
138383615483836155AG34GENIChomozygous777023571
138383686283836863TA28GENIChomozygous777023572
138383779883837799CG48GENIChomozygous777023573
138383878383838784TC46GENIChomozygous777023574
138383971383839714GA54GENIChomozygous777023575
138384199383841994CG25GENIChomozygous777023576
138384201083842011CA20GENICpossibly homozygous777023577