chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104333282243332823CCCTCTGTG19GENICheterozygous52495979
104333775843337759A-34GENICpossibly homozygous51435206
104334014943340150GGGTGT8GENIChomozygous51435210
104334087543340879TTTT----23GENICheterozygous52147696
104333343943333440TTG26GENIChomozygous52147686
104333500543335006GA17GENIChomozygous52147688
104333777143337772AC35GENICpossibly homozygous52147690
104333923743339242TGAGT-----16GENIChomozygous52147694
104334087843340879T-23GENICheterozygous51435211
104334130643341307GT21GENIChomozygous52147698
104334482143344822TC37GENIChomozygous51435214