chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139208238139208239AG5GENIChomozygous114028435
5139209251139209252GT6GENIChomozygous114028437
5139210249139210250AG23GENICpossibly homozygous114028438
5139210973139210974TC23GENIChomozygous114028439
5139212018139212019TC23GENIChomozygous114028441
5139212853139212854GA19GENIChomozygous114028442
5139213455139213456AG13GENIChomozygous114028443
5139214139139214140GA17GENIChomozygous114028444
5139214293139214294CT22GENIChomozygous114028445
5139215125139215126CT35GENIChomozygous114028446
5139215185139215186GA27GENIChomozygous114028447
5139215828139215829AG32GENIChomozygous114028448
5139216261139216262GA26GENIChomozygous114028449
5139217313139217314AG31GENIChomozygous114028450
5139218721139218722CA28GENIChomozygous114028451
5139218736139218737AG29GENIChomozygous114028452
5139219056139219057GA35GENIChomozygous114028453
5139219897139219898TG24GENIChomozygous114028454
5139220043139220044AG28GENIChomozygous114028455
5139220604139220605AG33GENIChomozygous114028456
5139222241139222242AG27GENIChomozygous114028458
5139224483139224484CA19GENIChomozygous114028461
5139225578139225579GA22GENIChomozygous114028462
5139226136139226137GT20GENIChomozygous114028463