chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG26GENICpossibly homozygous675175174
8121843359121843360CT22GENICpossibly homozygous675175175
8121843428121843429CT15GENICpossibly homozygous675175176
8121843478121843479AG18GENIChomozygous675175177
8121843825121843826GA34GENICpossibly homozygous675175178
8121844425121844426AC35GENIChomozygous675175179
8121844635121844636TC25GENIChomozygous675175180
8121845391121845392GGA3GENIChomozygous771223915
8121845798121845799GC31GENIChomozygous675175181
8121846799121846800TA29GENICpossibly homozygous675175182
8121846878121846879CT36GENICpossibly homozygous675175183
8121847281121847282A-16GENICheterozygous771223916
8121848181121848182CT14GENIChomozygous675175184
8121848295121848296AC26GENIChomozygous675175185