chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143820618143820619GA11GENICpossibly homozygous115944682
7143820791143820792AC12GENIChomozygous115944683
7143820831143820832AG13GENIChomozygous115944684
7143820874143820874TTTG11GENIChomozygous128531494
7143823278143823280AG22GENIChomozygous128531495
7143823581143823581G13GENIChomozygous128531496
7143823699143823700AG16GENIChomozygous115944685
7143824329143824330CT24GENIChomozygous115944686
7143825659143825659T19GENICheterozygous128531497
7143826120143826121GT27GENIChomozygous115944687
7143826854143826855GA19GENIChomozygous115944688
7143827011143827012AT22GENIChomozygous115944689
7143827261143827262AG14GENIChomozygous115944690
7143828599143828600GA28GENIChomozygous115944691
7143829200143829201GA17GENIChomozygous115944692
7143829469143829469AG22GENIChomozygous128531498
7143829736143829737AG20GENIChomozygous115944693
7143829754143829755AG20GENIChomozygous115944694
7143829823143829824C10GENIChomozygous128531499
7143829836143829837TC9GENIChomozygous115944695
7143829844143829845AG9GENIChomozygous115944696
7143829896143829896AAAGAAAGAAAG13GENIChomozygous128531500
7143829928143829929AG15GENIChomozygous115944699
7143829932143829933AG16GENIChomozygous115944700
7143830114143830115TC21GENIChomozygous115944701
7143830247143830248AG24GENIChomozygous115944702
7143830394143830394AATAGTCGAGTCTGTTA26GENIChomozygous128531501
7143830866143830867GA21GENIChomozygous115944703
7143833153143833154CT29GENIChomozygous115944704
7143833859143833860AG27GENIChomozygous115944705
7143834487143834488GA24GENIChomozygous115944706
7143834777143834778CT23GENIChomozygous115944707
7143837016143837017TC36GENIChomozygous115944708
7143837232143837233CT33GENIChomozygous115944709
7143837375143837376AG26GENIChomozygous115944710