chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105247380105247381AG6GENICheterozygous61491817
1105247469105247470AC18GENIChomozygous61491818
1105247573105247574GA22GENICpossibly homozygous61737449
1105247870105247871TC27GENICpossibly homozygous61491819
1105248153105248154CT7GENIChomozygous61737451
1105248173105248174G-4GENIChomozygous61737453
1105248437105248438GA16GENICpossibly homozygous61491820
1105249139105249140TC12GENICpossibly homozygous61491821
1105255006105255007CA1GENIChomozygous60780745
1105258515105258516TC34GENICpossibly homozygous61737461
1105259279105259280TC20GENICpossibly homozygous61737463
1105259584105259585AG10GENICheterozygous61737465
1105259760105259761GA18GENIChomozygous61737467
1105259837105259838CG4GENIChomozygous60780750
1105259856105259857CA5GENIChomozygous60780751
1105260236105260237AC27GENICpossibly homozygous61491829