chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG26GENIChomozygous593640492
8121843359121843360CT27GENIChomozygous593640493
8121843428121843429CT29GENIChomozygous593640494
8121843478121843479AG33GENIChomozygous593640495
8121843825121843826GA27GENIChomozygous593640496
8121844425121844426AC30GENIChomozygous595203433
8121844635121844636TC49GENIChomozygous593640497
8121845391121845392GGA2GENIChomozygous726166019
8121845798121845799GC20GENIChomozygous593640498
8121846799121846800TA34GENIChomozygous593640499
8121846878121846879CT34GENIChomozygous593640500
8121847281121847282A-11GENICpossibly homozygous726166020
8121848181121848182CT17GENIChomozygous595203434
8121848295121848296AC26GENIChomozygous595203435