chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105245880105245881CCA22GENIChomozygous61491815
1105246243105246244AT26GENIChomozygous61491816
1105247380105247381AG18GENIChomozygous61491817
1105247469105247470AC27GENIChomozygous61491818
1105247870105247871TC22GENIChomozygous61491819
1105248437105248438GA24GENIChomozygous61491820
1105249139105249140TC27GENIChomozygous61491821
1105249642105249644AC--26GENIChomozygous61491822
1105249647105249648C-26GENIChomozygous61491823
1105250683105250684CCGT7GENICheterozygous60780743
1105250684105250686GT--7GENICheterozygous60780744
1105251029105251030GA15GENIChomozygous61491824
1105251807105251808CT22GENIChomozygous61491825
1105255006105255007CA4GENIChomozygous60780745
1105255928105255929CCTT4GENICheterozygous61491826
1105256868105256872CACA----8GENICpossibly homozygous60780746
1105256870105256872CA--8GENICheterozygous60780747
1105256916105256917C-14GENICheterozygous60780748
1105259091105259092CA14GENIChomozygous61491827
1105259095105259096TA14GENIChomozygous61491828
1105260236105260237AC26GENIChomozygous61491829
1105260422105260423TC20GENIChomozygous61491830
1105260873105260874TTA11GENIChomozygous61491831
1105257365105257366G-23GENIChomozygous60780749
1105259837105259838CG28GENIChomozygous60780750
1105259856105259857CA29GENIChomozygous60780751