chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75728147557281476TC42GENICheterozygous116291091
75728149057281491AT41GENICheterozygous116291092
75728150057281501GC48GENICheterozygous116291093
75730528057305281GA158GENICheterozygous116291094
75738193257381933GT49GENICpossibly homozygous116291095
75739488157394882TG41GENIChomozygous115688340
75738212157382122TA39GENIChomozygous115688337
75738214057382141AG48GENIChomozygous115688338
75739523257395233AC40GENIChomozygous115688341
75749026357490264AC92GENICheterozygous116291096
75749118957491190AG58GENICheterozygous115688344
75749121157491212GA56GENICheterozygous115688345
75749122757491228CT60GENICheterozygous115688346
75749126557491266AG55GENICheterozygous115688347
75752761457527615CA49GENIChomozygous115688349
75758374757583748GT39GENICheterozygous116291097
75762158957621590CA16GENICheterozygous115688350
75764765557647656CG15GENIChomozygous116291098
75764785157647852AG25GENIChomozygous115688351
75764789257647893CT32GENIChomozygous115688352
75764789457647895CA32GENIChomozygous115688353
75764789657647897CT35GENIChomozygous115688354
75764794957647950TG54GENICpossibly homozygous115688355
75765567557655676AG44GENIChomozygous115688356
75765573557655736AC48GENIChomozygous115688357
75765582857655829AC10GENICpossibly homozygous115688358
75765603757656038TA19GENIChomozygous116027874
75765626457656265GT19GENIChomozygous115688359