chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72896636128966363GT12GENICheterozygous130342067
72900892329008924TC9GENIChomozygous116326045
72900982529009826AG17GENIChomozygous116131311
72901032229010323TC18GENIChomozygous116131317
72901575729015758AG22GENIChomozygous116131327
72901118329011184GA29GENIChomozygous116326046
72901313929013140CT10GENIChomozygous116326047
72901072029010738TGTGTATGTGTGTATGTG11GENIChomozygous131009936
72901177729011777T14GENIChomozygous131009937
72901304529013045T14GENICpossibly homozygous131009938
72901588629015887GA25GENIChomozygous116326049
72901687429016875AG11GENIChomozygous118276112
72901687529016876GA11GENIChomozygous118276113
72901879629018797AG19GENIChomozygous118276114
72901879729018798GA19GENIChomozygous118276115
72901920729019208CT12GENIChomozygous116131335
72901934929019350GA19GENIChomozygous116131337
72901960029019601TC17GENIChomozygous116131339
72901963829019639AT17GENIChomozygous116326050
72901976329019764GA18GENIChomozygous116131341
72901994429019945CA10GENIChomozygous116131343
72902107729021077CGGAG16GENIChomozygous131009939
72902138129021382GC14GENIChomozygous116131345
72902208129022082AG16GENIChomozygous116131347
72902247529022476AG11GENIChomozygous116131349
72902279529022796GA8GENIChomozygous116131351
72902022929020230CT13GENIChomozygous116326051