chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45647961956479620G38GENIChomozygous128036395
45647967456479675TC44GENIChomozygous112656861
45647998256479983GA61GENIChomozygous112656862
45648015156480152GA47GENIChomozygous112656863
45648115456481155CT50GENIChomozygous112656864
45648509156485092C48GENIChomozygous128036396
45648516256485163GA42GENIChomozygous112656868
45648178056481781TC39GENIChomozygous112656865
45648199056481991TC40GENIChomozygous112656866
45648432756484328AG43GENIChomozygous112656867
45648560656485606TT24GENIChomozygous128036397
45648573556485736AT10GENICheterozygous133952356
45648641556486416GA38GENIChomozygous112656869
45648794556487945GAGGCA27GENIChomozygous128036398
45649075456490755GA29GENIChomozygous112656870
45649155956491559A56GENIChomozygous128036399
45649170556491706TC35GENIChomozygous112656871
45649204356492044AG37GENIChomozygous112656872
45649209056492090CCCACCT32GENICpossibly homozygous128036400
45649066956490670CG6GENICheterozygous128125446
45649067156490672CG5GENIChomozygous128125447