chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152241902222419023CCTT10GENICheterozygous48255434
152241904722419048CT22GENICheterozygous48255435
152242538022425381A-13GENICheterozygous48255450
152243556822435569TC30GENIChomozygous48255469
152243870722438714TTTTTTC-------9GENICheterozygous48255474
152243883222438833GGT10GENIChomozygous48255475
152243928222439283TTACACACACAC11GENICheterozygous48255476
152243982722439828CCA19GENIChomozygous48255478
152244072822440730AA--8GENICpossibly homozygous48255479
152244076422440765GC21GENICheterozygous48255480
152244745822447459GGA18GENICheterozygous48255506
152244767422447676GT--3GENIChomozygous48255507
152244902122449022G-10GENICheterozygous48255513
152244903322449034T-11GENICheterozygous48255514