chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
54785415547854156AT56GENIChomozygous113786285
54785804347858044AT45GENIChomozygous113786287
54786548647865487TA56GENIChomozygous113786296
54786571747865718CT56GENIChomozygous113786298
54786691647866917TC53GENIChomozygous113786300
54787614247876143TC57GENIChomozygous113786303
54786184747861848GA51GENIChomozygous119159129
54786898247868983TC56GENIChomozygous119159131
54786355247863559TTTGTTT39GENIChomozygous128179201
54786418247864184TC25GENICpossibly homozygous131382735
54788360747883608CT5GENIChomozygous113786309
54788421447884215TC68GENICheterozygous113786313
54788421947884220GA67GENICheterozygous113786315
54788423447884235TC66GENICheterozygous113786317
54788424447884245GA62GENICheterozygous113786319
54788439447884395CT13GENICheterozygous128285322
54786637547866375TTAT48GENICpossibly homozygous128179202
54788410147884104GTT26GENICpossibly homozygous128179205
54788395947883960GA17GENICheterozygous130319046
54788418247884183GA68GENICheterozygous128285318
54788420447884205AG69GENICheterozygous128285319
54788420547884206CG69GENICheterozygous128285320
54788420847884209CG69GENICheterozygous128285321
54788451047884511GA21GENICheterozygous132085074
54788458147884582GT30GENICheterozygous128285325
54788486047884861TC36GENICheterozygous122291550
54788494047884941TC39GENICheterozygous113786321
54788722747887228GA59GENIChomozygous119159133
54788791747887917T36GENIChomozygous128179208
54788806547888066CT58GENIChomozygous119159134
54788991847889918A50GENIChomozygous128179209
54788459547884596TG31GENICheterozygous131859685