chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187355104973551050TC39GENIChomozygous110401522
187355120573551206AG45GENIChomozygous110401524
187355155273551553TA41GENIChomozygous110401526
187355180073551801TC39GENIChomozygous110401528
187355382373553824AG50GENIChomozygous110401530
187355573473555735CT24GENIChomozygous110401532
187355673473556735TC37GENIChomozygous110401534
187355694673556947CG41GENIChomozygous110401536
187355754973557550CT38GENIChomozygous110401538
187355805473558055GA45GENIChomozygous110401540
187355812073558121TC54GENIChomozygous110401542
187355943773559438CT53GENIChomozygous110401544
187355979673559797CT33GENIChomozygous110401546
187355996973559970AG38GENIChomozygous110401548
187356000673560007GA43GENIChomozygous110401550
187356011873560119CT57GENIChomozygous110401552
187356024673560247TC40GENIChomozygous110401554
187356076973560770CA42GENIChomozygous110401556
187356106573561066CT42GENIChomozygous110401558
187356140073561401TG59GENIChomozygous110401560
187356146473561465TC57GENIChomozygous110401562
187356193573561936TC40GENIChomozygous110401564
187356226173562262CT36GENIChomozygous110401566
187356391073563911CG25GENIChomozygous110401568
187356725473567255TC55GENIChomozygous110401570
187356925173569252TC46GENIChomozygous110401572
187356925873569259GC46GENIChomozygous110401574
187356960873569609CT42GENIChomozygous110401576
187357019573570196TC32GENIChomozygous110401578
187357027273570273TA37GENIChomozygous110401580
187357220073572201CT59GENIChomozygous110401583
187357256273572563TC18GENIChomozygous110401585
187357384873573849AG34GENIChomozygous110401586
187357394073573941CT28GENIChomozygous110401588
187357435573574356TC47GENIChomozygous110401590
187357449373574494TC31GENIChomozygous110401592