chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250710102250710103TC30GENIChomozygous111292764
2250710380250710381AG28GENIChomozygous111292765
2250710482250710483CT25GENIChomozygous111292766
2250717249250717250AG27GENIChomozygous111292767
2250720077250720078GC33GENIChomozygous110915018
2250720882250720883CT42GENIChomozygous111292769
2250724143250724144TC40GENIChomozygous110379621
2250725211250725212AG23GENIChomozygous110379625
2250726488250726489AC23GENIChomozygous111292771
2250727501250727502CT22GENIChomozygous111292772
2250728211250728212AG19GENIChomozygous110379633
2250728365250728366CT19GENIChomozygous111292773
2250729179250729180AT22GENIChomozygous120163497
2250729180250729181TA22GENIChomozygous120163498
2250729654250729655GA20GENIChomozygous110379635
2250729916250729917GA25GENIChomozygous111292774
2250730274250730275GA28GENIChomozygous110379639
2250730508250730509TC29GENICpossibly homozygous110379643
2250730986250730987CA27GENIChomozygous110379645
2250731668250731669TC21GENIChomozygous110379647
2250733489250733490CT34GENIChomozygous110379649
2250733952250733953GA21GENIChomozygous111292775
2250734373250734374CT13GENIChomozygous111292776
2250734722250734723AG18GENIChomozygous110379651
2250734870250734871AC17GENIChomozygous110379653
2250735468250735469TC17GENIChomozygous110379655
2250737293250737294GA21GENIChomozygous110379657
2250738025250738026AT17GENIChomozygous120300345
2250738026250738027TG17GENIChomozygous120300346
2250738043250738044GT15GENIChomozygous110379663
2250739894250739895TC20GENIChomozygous111292777
2250742455250742456AC43GENIChomozygous110379665