chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106691461166914612TC50GENIChomozygous51679443
106691569466915695GA32GENIChomozygous51909059
106692095366920954TC41GENIChomozygous51679489
106692189266921893CT8GENIChomozygous51679499
106692230466922305AC13GENIChomozygous51909061
106692323266923233GA72GENICpossibly homozygous51909063
106692350066923501AG50GENIChomozygous51909065
106692505566925071ACACACACACACACAC----------------11GENICpossibly homozygous51679515
106692532166925322TTAAAG29GENIChomozygous51679519
106692831466928321ATATATA-------20GENIChomozygous51679545
106693372366933724CT37GENIChomozygous51679590
106693655866936559CCAG36GENICpossibly homozygous51679604
106693656066936561CG51GENICheterozygous51679606
106693658666936587CA43GENICheterozygous51909067
106693658666936587CCAA27GENIChomozygous51909069
106693878066938781TTATAC3GENICheterozygous51679621
106693878066938781TTAC3GENICheterozygous51909071
106693917766939181AGAG----3GENIChomozygous51679623
106693953166939532TG38GENIChomozygous51679629
106694212766942128TC15GENIChomozygous51679635
106694316066943161AT25GENICpossibly homozygous51987910