chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221185340221185341AATGTGTGTG11GENIChomozygous62101899
1221186371221186373AA--8GENICheterozygous61093772
1221189551221189552GA7GENIChomozygous62589484
1221190097221190098G-7GENIChomozygous61093776
1221190111221190112A-7GENIChomozygous62355182
1221190831221190832AC24GENICpossibly homozygous61321158
1221191017221191018AAT22GENICpossibly homozygous61093781
1221191684221191685CT29GENIChomozygous62589485
1221191017221191018AATT22GENICheterozygous62414469