chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167473099874730998A24GENICheterozygous129382041
167473484674734847GT16GENIChomozygous119129704
167473484974734850AG16GENIChomozygous119129706
167473486074734860AGACAAATAAAAAGGGAAGGAGAGGGTAGTAAAAGACAGTAAGGGTATCTGAAGAGTCATGAGAAAAATGTGACAGTACTCACTCCAGAGCCAC20GENIChomozygous129382047
167474065574740655A34GENIChomozygous129382052
167474066174740661A32GENIChomozygous129382053
167474074874740749G23GENIChomozygous129382054
167474081874740818A29GENIChomozygous129382055
167474082574740825G26GENIChomozygous129382056
167474086974740869T36GENIChomozygous129382057
167474089474740895GT36GENIChomozygous111861680
167474092174740922C30GENIChomozygous129382058
167474093774740937G30GENIChomozygous129382059
167474100674741006T16GENIChomozygous129382060
167474103174741031C13GENIChomozygous129382061
167474118574741185C23GENIChomozygous129382062
167474121274741213G25GENICheterozygous130597273
167474122774741228T30GENIChomozygous129382063
167474123674741236A24GENIChomozygous129382064
167474123974741239T29GENIChomozygous129382065
167474124974741249A32GENIChomozygous129382066
167474126174741264GCA32GENIChomozygous129382067