chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250785784250785785GC26GENICheterozygous110850867
2250787124250787125TA7GENIChomozygous110379826
2250793920250793921AT23GENIChomozygous110379840
2250794497250794498AG16GENIChomozygous110379844
2250795651250795652CT16GENIChomozygous110850876
2250796670250796671GA16GENIChomozygous110850878
2250798466250798467TA12GENIChomozygous110379856
2250800397250800398GA11GENIChomozygous110850880
2250800721250800722AT5GENIChomozygous110379860
2250800778250800779GA5GENIChomozygous110850882
2250800812250800813TA4GENIChomozygous110850886
2250800872250800873CA6GENIChomozygous110850888
2250800915250800916TC10GENIChomozygous110850892
2250801069250801070CT7GENICheterozygous110850894
2250801489250801490AT12GENIChomozygous110850897
2250801712250801713TA18GENIChomozygous110850899
2250801739250801740GA22GENIChomozygous110850901
2250801884250801885CT15GENIChomozygous110850903
2250801938250801939TC5GENIChomozygous110850905
2250802081250802082AG19GENIChomozygous110379861
2250802357250802358AG18GENIChomozygous110850907
2250802533250802534AG13GENIChomozygous110850909
2250802564250802565AC19GENIChomozygous110850911
2250804353250804354AG12GENIChomozygous110379865