chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100396756100396757CT47GENIChomozygous113284058
4100397042100397042ACTG38GENIChomozygous130935479
4100397744100397745CG39GENIChomozygous112798591
4100397750100397751CG35GENIChomozygous112798593
4100397772100397773CA33GENIChomozygous112798595
4100397790100397791AG33GENIChomozygous112798597
4100397796100397797GA31GENIChomozygous112798599
4100397812100397813GT31GENIChomozygous112798601
4100397824100397824G29GENIChomozygous128063679
4100397830100397831TA29GENIChomozygous112798603
4100397841100397842GA26GENIChomozygous112798605
4100397852100397853GA25GENIChomozygous112798607
4100399521100399521G52GENIChomozygous130935481
4100402925100402925TT25GENIChomozygous131357472
4100405077100405078A43GENICheterozygous130935486
4100405090100405091AG50GENIChomozygous112798609
4100407400100407414AGGGAAGAGGGGAA9GENIChomozygous131357473
4100412201100412202AG46GENIChomozygous113284084
4100417982100417983TC57GENIChomozygous113284089
4100418004100418005AT54GENIChomozygous113284090
4100418355100418356G55GENIChomozygous128063680
4100418586100418587C45GENIChomozygous128063681
4100418591100418591T45GENIChomozygous128063682
4100418600100418601A45GENIChomozygous128063683
4100418607100418607A47GENIChomozygous128063684
4100416663100416664CT51GENIChomozygous132067437
4100418615100418616TC50GENIChomozygous112798611
4100397865100397866TC28GENIChomozygous119499509
4100397866100397867GT28GENIChomozygous119279528
4100402332100402333AG40GENIChomozygous119344163
4100413018100413019TG36GENIChomozygous119344165
4100402908100402908CTTC23GENIChomozygous132058570
4100406900100406901GA35GENIChomozygous113537586
4100414965100414966TG37GENIChomozygous113537588
4100415428100415429AC17GENICpossibly homozygous113537590