chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
149563204595632046CA35GENIChomozygous139597223
149563541695635417CT70GENICpossibly homozygous139597224
149563599195635992CT36GENIChomozygous139597225
149563702595637026CT43GENIChomozygous139597226
149563732395637324AT34GENIChomozygous139597227
149563733195637332AC33GENIChomozygous139597228
149563733495637335TC33GENIChomozygous139597229
149563733695637337GA32GENIChomozygous139597230
149563755695637557TA68GENIChomozygous139597231
149563766795637668CT54GENIChomozygous139597232
149563799895637999TC47GENIChomozygous139597233
149563804695638047AC46GENIChomozygous139597234
149563809495638095CT51GENIChomozygous139597235
149563932995639330TC44GENIChomozygous139597236
149563940295639403TC48GENIChomozygous139597237
149564302295643023GA51GENIChomozygous139597238
149564320995643210CT41GENIChomozygous139597239
149564425895644259TC42GENIChomozygous139597240
149564499195644992AG49GENIChomozygous139597241
149564539495645395CT57GENIChomozygous139597242
149563506195635061A47GENIChomozygous139411313
149563490395635015AAAAACTTCTGAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAAA36GENIChomozygous139411312