chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74693341446933415CT54GENIChomozygous138084667
74693420946934210CT41GENIChomozygous138084668
74693590646935907TC56GENIChomozygous138084669
74693859946938600GA54GENIChomozygous138084670
74693974646939747TA69GENIChomozygous138084671
74694031546940316CT63GENIChomozygous138084672
74694192546941926GA56GENIChomozygous138084673
74694245246942453TC52GENIChomozygous138084674
74693600346936003G52GENIChomozygous137952097
74694191646941920TTTC53GENIChomozygous137952098
74694370546943706CA71GENIChomozygous138084675
74694407746944078GA63GENIChomozygous138084676
74694470446944705AG64GENIChomozygous138084677
74694514746945151TGTT63GENIChomozygous137952099
74695050546950506CT55GENIChomozygous138084678
74695052446950525TC53GENIChomozygous138084679
74695205746952058CT50GENIChomozygous138084680
74695208946952090TG43GENIChomozygous138084681
74695414946954150AG56GENIChomozygous138084682
74695449146954492GA43GENIChomozygous138084683
74695512746955128CT53GENIChomozygous138084684
74695520946955210TG50GENIChomozygous138084685
74695636146956362AG49GENIChomozygous138084686
74695023146950231T53GENIChomozygous137952100
74695671646956718GT39GENIChomozygous137952101
74695710146957101T38GENIChomozygous137952102