chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5119050135119050136TC30GENIChomozygous55663859
5119052154119052155CG49GENICheterozygous55663861
5119052302119052303CG71GENICheterozygous55663863
5119052446119052447GA130GENICheterozygous55663865
5119053565119053566GA71GENICheterozygous55663867
5119053841119053842AC18GENICpossibly homozygous55663869
5119054023119054024AG16GENICpossibly homozygous55663871
5119054090119054091A-2GENIChomozygous55663873
5119054319119054320GA26GENIChomozygous55663875
5119054330119054331CT25GENIChomozygous55663877
5119054761119054762TG32GENIChomozygous55663879
5119055350119055351A-23GENIChomozygous55663881
5119055369119055370GA26GENIChomozygous55663882
5119056193119056194AG59GENIChomozygous55663884
5119058417119058418GA41GENICpossibly homozygous55663886
5119060466119060467CT42GENIChomozygous55663888
5119061102119061103AC50GENIChomozygous55663890
5119063196119063198CA--6GENIChomozygous55663892
5119063200119063204ACCA----6GENIChomozygous55663893
5119065172119065173AAGTGTGTGT9GENIChomozygous55663895
5119065461119065462AG56GENIChomozygous55663897
5119067159119067160TC28GENIChomozygous55663898
5119068306119068307CCTTT5GENIChomozygous55663900
5119069262119069263CT16GENIChomozygous55663901
5119069269119069270GT16GENIChomozygous55663903