chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187355120573551206AG27GENIChomozygous110401524
187355155273551553TA28GENIChomozygous110401526
187355180073551801TC21GENIChomozygous110401528
187355382373553824AG30GENIChomozygous110401530
187355573473555735CT37GENIChomozygous110401532
187355673473556735TC16GENIChomozygous110401534
187355694673556947CG42GENIChomozygous110401536
187355754973557550CT41GENIChomozygous110401538
187355805473558055GA29GENIChomozygous110401540
187355812073558121TC39GENIChomozygous110401542
187355943773559438CT30GENIChomozygous110401544
187355979673559797CT25GENIChomozygous110401546
187355996973559970AG23GENIChomozygous110401548
187356000673560007GA28GENIChomozygous110401550
187356011873560119CT25GENIChomozygous110401552
187356024673560247TC28GENIChomozygous110401554
187356076973560770CA26GENIChomozygous110401556
187356106573561066CT20GENIChomozygous110401558
187356140073561401TG33GENIChomozygous110401560
187356146473561465TC26GENIChomozygous110401562
187356193573561936TC34GENIChomozygous110401564
187356206773562068TC24GENIChomozygous110499668
187356725473567255TC28GENIChomozygous110401570
187356925173569252TC25GENIChomozygous110401572
187356925873569259GC23GENIChomozygous110401574
187356960873569609CT33GENIChomozygous110401576
187357019573570196TC33GENIChomozygous110401578
187357027273570273TA34GENIChomozygous110401580
187357220073572201CT22GENIChomozygous110401583
187357256273572563TC19GENIChomozygous110401585
187357384873573849AG27GENIChomozygous110401586
187357394073573941CT15GENIChomozygous110401588
187357435573574356TC36GENIChomozygous110401590
187357449373574494TC17GENIChomozygous110401592