chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130542700130542701GT13INTERGENIChomozygous54242204
7130542978130542979CT15INTERGENIChomozygous54111923
7130543297130543299CA--3INTERGENICheterozygous54111925
7130544013130544014GA17INTERGENICpossibly homozygous54242208
7130544677130544678CT23INTERGENIChomozygous54242210
7130544848130544849TC10INTERGENICpossibly homozygous54111933
7130545256130545257TC22INTERGENIChomozygous54111937
7130545283130545284C-8INTERGENIChomozygous54242214
7130545286130545289TCC---10INTERGENIChomozygous54242216
7130546467130546468AT3INTERGENIChomozygous54111941
7130546513130546514GA16INTERGENICheterozygous54111942
7130546809130546810CT10INTERGENIChomozygous54242221
7130546903130546904TC29INTERGENIChomozygous54111953
7130548044130548045AT2INTERGENIChomozygous54111954
7130548076130548077AT3INTERGENIChomozygous54111955
7130548089130548090CA2INTERGENIChomozygous54111957
7130548243130548244CA11INTERGENICpossibly homozygous54111959
7130548310130548311GA13INTERGENICpossibly homozygous54242223