chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130542700130542701GT24INTERGENIChomozygous54242204
7130542978130542979CT35INTERGENIChomozygous54111923
7130543283130543287AAAA----13INTERGENIChomozygous54242206
7130543297130543299CA--14INTERGENIChomozygous54111925
7130544013130544014GA26INTERGENIChomozygous54242208
7130544677130544678CT24INTERGENIChomozygous54242210
7130544848130544849TC18INTERGENIChomozygous54111933
7130545256130545257TC28INTERGENIChomozygous54111937
7130545283130545284C-20INTERGENIChomozygous54242214
7130545286130545289TCC---23INTERGENIChomozygous54242216
7130546282130546286TATG----13INTERGENIChomozygous54242218
7130546467130546468AT17INTERGENIChomozygous54111941
7130546513130546514GA18INTERGENIChomozygous54111942
7130546697130546698CCCTG9INTERGENICpossibly homozygous55010555
7130546700130546701GGGAGAAGGTGTGGTCCTGTTGGAGTAGGTGGGGTCCTGTTGGAGAAGGTGTGGTCCTGTTGGAGTAGGTGTGGTCTTATTGGAGTAGGTGTGGTCTTA9INTERGENICpossibly homozygous55010557
7130546809130546810CT34INTERGENIChomozygous54242221
7130546903130546904TC19INTERGENIChomozygous54111953
7130548044130548045AT20INTERGENIChomozygous54111954
7130548076130548077AT22INTERGENIChomozygous54111955
7130548089130548090CA22INTERGENIChomozygous54111957
7130548243130548244CA23INTERGENIChomozygous54111959
7130548310130548311GA20INTERGENIChomozygous54242223