chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221185340221185341AATGTGTGTG14GENICpossibly homozygous62101899
1221186371221186373AA--5GENICheterozygous61093772
1221189551221189552GA16GENIChomozygous62589484
1221190097221190098G-8GENIChomozygous61093776
1221190111221190112A-7GENIChomozygous62355182
1221190831221190832AC22GENIChomozygous61321158
1221191017221191018AAT23GENICpossibly homozygous61093781
1221191684221191685CT24GENICpossibly homozygous62589485