chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55778776157787762AG14GENIChomozygous137477219
55778959957789600TC23GENICpossibly homozygous137477220
55778978057789781GA31GENIChomozygous137477221
55778973557789735A25GENIChomozygous137310389
55779413757794138TC19GENIChomozygous137477222
55779508857795089TC24GENIChomozygous137477223
55779515357795154GA24GENIChomozygous137477224
55779650357796504GA15GENIChomozygous137477225
55779657857796578A15GENIChomozygous137310390
55779681657796816G22GENIChomozygous137310391
55779769457797694C22GENIChomozygous137310392
55779778357797784A24GENIChomozygous137310393
55779780157797802AG17GENIChomozygous137477227
55779837057798371AG30GENIChomozygous137477228
55779959957799600GT28GENIChomozygous137477229
55780032557800325AGTCGACCCTCTTGG29GENIChomozygous137310394
55780424957804250CT26GENIChomozygous137477230
55780443557804436AG25GENICpossibly homozygous137477231
55780478157804782GA26GENICpossibly homozygous137477232
55780486357804864CT25GENIChomozygous137477233
55780504157805041A29GENIChomozygous137310395
55780504257805043GA29GENIChomozygous137477235
55780506557805066TC36GENIChomozygous137477236
55780544357805444CT21GENIChomozygous137477237
55780574457805745TC21GENIChomozygous137477238
55780598057805981AG8GENIChomozygous137477239
55780693457806935TA24GENICpossibly homozygous137477240
55780693957806940CT25GENICpossibly homozygous137477241
55780695257806953CT26GENICpossibly homozygous137477242
55780785957807860TC25GENIChomozygous137477243
55780857657808577TC21GENIChomozygous137477244
55781015457810155CA21GENIChomozygous137477245
55781042457810424T16GENIChomozygous137310396
55781042557810426AC17GENIChomozygous137477246
55781053857810539CT23GENIChomozygous137477247
55781069357810694CT20GENIChomozygous137477248
55781399757813998CT8GENIChomozygous137477249
55781560657815607AG10GENIChomozygous137477250
55781634057816340T12GENIChomozygous137310398
55781688257816883AT19GENIChomozygous137477251