chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2123696729123696730TG17GENIChomozygous136275120
2123697083123697084GA15GENIChomozygous136275121
2123697421123697422AG19GENIChomozygous136275122
2123697803123697804AG26GENIChomozygous136275123
2123698193123698194CA26GENIChomozygous136275124
2123698397123698397T18GENIChomozygous135940542
2123698465123698466TC20GENIChomozygous136275125
2123699047123699048T17GENIChomozygous135940543
2123699324123699325AG18GENIChomozygous136275126
2123699936123699942ATTCTA19GENIChomozygous135940544
2123700275123700276TC24GENIChomozygous136275127
2123700923123700924CT15GENIChomozygous136275128
2123701538123701539AG25GENIChomozygous136275129
2123701979123701980CT21GENIChomozygous136275130
2123702344123702345AG24GENIChomozygous136275131
2123702757123702758CT19GENIChomozygous136275132
2123704404123704406AA19GENIChomozygous135940545
2123704407123704446GAAATACATAGGTAATGCCACTGATTTATTTTCCAACTC20GENIChomozygous135940546
2123704470123704471GA24GENIChomozygous136275133
2123706369123706369G16GENIChomozygous135940547
2123706983123706984T19GENIChomozygous135940548
2123708670123708670TG26GENIChomozygous135940549
2123709361123709362TA23GENIChomozygous136275134
2123709537123709538AG18GENIChomozygous136275135
2123709780123709781AG17GENIChomozygous136275136
2123709929123709929TGTGGGA18GENIChomozygous135940550