chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225164117225164118GA17GENICpossibly homozygous109450298
1225164633225164634TG6GENIChomozygous120848980
1225166365225166366CT12GENIChomozygous109450299
1225166916225166917AG16GENIChomozygous108556572
1225169033225169034AG17GENICheterozygous108771597
1225169041225169042TG15GENICheterozygous108771598
1225169077225169078GA16GENICheterozygous109056961
1225169078225169079CT16GENICheterozygous109056962
1225169087225169088GA15GENICheterozygous109056963
1225169877225169878CT23GENIChomozygous120595365
1225169895225169896TA21GENIChomozygous120595367