chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG12GENIChomozygous671383461
8121843359121843360CT20GENICpossibly homozygous671383462
8121843428121843429CT16GENIChomozygous671383463
8121843478121843479AG23GENIChomozygous671383464
8121843825121843826GA20GENICheterozygous671383465
8121844425121844426AC20GENICpossibly homozygous671383466
8121844635121844636TC10GENICpossibly homozygous671383467
8121845798121845799GC9GENICpossibly homozygous671383468
8121846799121846800TA12GENICheterozygous671383469
8121846878121846879CT17GENIChomozygous671383470
8121848181121848182CT15GENIChomozygous671383471
8121848295121848296AC13GENIChomozygous671383472