chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143820618143820619GA36GENIChomozygous115944682
7143820791143820792AC53GENIChomozygous115944683
7143820831143820832AG52GENIChomozygous115944684
7143823699143823700AG43GENIChomozygous115944685
7143824329143824330CT45GENIChomozygous115944686
7143825659143825659T31GENICheterozygous128531497
7143820874143820874TTTG38GENIChomozygous128531494
7143823278143823280AG32GENIChomozygous128531495
7143823581143823581G25GENIChomozygous128531496
7143826120143826121GT60GENIChomozygous115944687
7143826854143826855GA49GENIChomozygous115944688
7143827011143827012AT40GENIChomozygous115944689
7143827261143827262AG22GENIChomozygous115944690
7143828599143828600GA47GENIChomozygous115944691
7143829200143829201GA53GENIChomozygous115944692
7143829469143829469AG41GENIChomozygous128531498
7143829736143829737AG49GENIChomozygous115944693
7143829754143829755AG44GENIChomozygous115944694
7143829823143829824C39GENIChomozygous128531499
7143829836143829837TC40GENIChomozygous115944695
7143829844143829845AG39GENIChomozygous115944696
7143829896143829896AAAGAAAGAAAG38GENIChomozygous128531500
7143829928143829929AG39GENIChomozygous115944699
7143829932143829933AG41GENIChomozygous115944700
7143830114143830115TC45GENIChomozygous115944701
7143830247143830248AG51GENIChomozygous115944702
7143830394143830394AATAGTCGAGTCTGTTA48GENIChomozygous128531501
7143830866143830867GA63GENIChomozygous115944703
7143833153143833154CT54GENIChomozygous115944704
7143833859143833860AG40GENIChomozygous115944705
7143834487143834488GA45GENIChomozygous115944706
7143834777143834778CT44GENIChomozygous115944707
7143836286143836287C14GENICpossibly homozygous128531503
7143837016143837017TC49GENIChomozygous115944708
7143837232143837233CT58GENIChomozygous115944709
7143837375143837376AG60GENIChomozygous115944710
7143835849143835850GA23GENICheterozygous128564430