chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2113547873113547874AG26GENIChomozygous59026940
2113547979113547980CT10GENIChomozygous59026941
2113548119113548120CT10GENIChomozygous59026942
2113548470113548471TA18GENIChomozygous59846045
2113549243113549244GA31GENICpossibly homozygous59026943
2113549333113549334CA32GENIChomozygous59026944
2113549866113549868AT--13GENIChomozygous59026945
2113549958113549959AG21GENIChomozygous59026946
2113550458113550459GA26GENICpossibly homozygous59846046
2113550879113550880TC23GENIChomozygous59026947
2113550892113550893TC23GENIChomozygous59026948
2113551241113551242TC9GENICheterozygous59026951
2113551697113551698GA27GENIChomozygous59026958
2113551957113551958CT33GENIChomozygous59846048
2113552228113552229GGT14GENICpossibly homozygous59026960
2113551639113551640T-13GENIChomozygous60449252
2113551641113551686ATGCAGTCAGGCTCCACCCTCTCATGTAGTCAGGCTCCACCCTCT---------------------------------------------14GENIChomozygous60449253
2113552255113552256CG21GENIChomozygous59846049
2113552274113552275TC20GENIChomozygous59846050