chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105245880105245881CCA11GENIChomozygous61491815
1105246162105246163AATGTGTGTGTGTG5GENIChomozygous62148307
1105246243105246244AT18GENIChomozygous61491816
1105247380105247381AG24GENIChomozygous61491817
1105247469105247470AC32GENIChomozygous61491818
1105247870105247871TC22GENIChomozygous61491819
1105248437105248438GA25GENIChomozygous61491820
1105249139105249140TC27GENIChomozygous61491821
1105249642105249644AC--15GENICpossibly homozygous61491822
1105250683105250684CCGTGT14GENICheterozygous61671027
1105250683105250684CCGTGTGT14GENICheterozygous61737455
1105250684105250686GT--14GENICheterozygous60780744
1105251029105251030GA26GENIChomozygous61491824
1105251807105251808CT21GENIChomozygous61491825
1105255006105255007CA4GENIChomozygous60780745
1105255009105255015CCCCCC------5GENIChomozygous62148311
1105255014105255015CCGGGGGG5GENIChomozygous62148313
1105259091105259092CA23GENIChomozygous61491827
1105259095105259096TA24GENIChomozygous61491828
1105259837105259838CG20GENIChomozygous60780750
1105259856105259857CA20GENIChomozygous60780751
1105260236105260237AC32GENIChomozygous61491829
1105260422105260423TC29GENIChomozygous61491830
1105260873105260874TTA6GENIChomozygous61491831