chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126196241126196242TC67GENIChomozygous119016641
5126196331126196332CT51GENIChomozygous119181886
5126196351126196352AG42GENIChomozygous119181887
5126196486126196487CG31GENIChomozygous119016642
5126197589126197590AG33GENIChomozygous119016643
5126197842126197843GC37GENIChomozygous119181888
5126198484126198485GT29GENIChomozygous113996642
5126198694126198695AG64GENIChomozygous113996644
5126198854126198855AG49GENIChomozygous119016646
5126199494126199495GT26GENIChomozygous119181889
5126204743126204744AT13GENIChomozygous119204072
5126206686126206687AT22GENIChomozygous113996652
5126207082126207083GA20GENIChomozygous119181890
5126207378126207379CT35GENIChomozygous119016652
5126208062126208063CT25GENIChomozygous113996654
5126208177126208178GA31GENIChomozygous119016654
5126208411126208412GA58GENICpossibly homozygous113996658
5126208590126208591TA49GENIChomozygous113996660
5126209139126209140GA29GENIChomozygous113996662
5126209488126209489AG49GENIChomozygous119016658
5126210065126210066TA24GENIChomozygous113996675
5126210445126210446AG57GENIChomozygous119016659
5126210514126210515AG27GENIChomozygous113996677
5126210631126210632TA40GENIChomozygous113996679
5126210670126210671TC46GENIChomozygous119181892
5126210873126210874TC38GENIChomozygous113996681
5126211601126211602CA12GENIChomozygous113996683
5126211773126211774AG43GENIChomozygous119181893
5126212671126212672AG42GENIChomozygous113996687
5126213292126213293GA58GENIChomozygous119181894
5126214852126214853AG39GENIChomozygous119181895
5126215383126215384CT25GENIChomozygous119181896
5126218507126218508CG36GENIChomozygous119204073
5126219108126219109AC31GENIChomozygous113996695
5126219664126219665CT51GENIChomozygous119181897
5126219778126219779TC33GENIChomozygous113996697
5126220418126220419CG70GENIChomozygous119181898
5126220467126220468AC79GENIChomozygous113996701