chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171537205171537206GC31GENIChomozygous60942828
1171538108171538109TC29GENIChomozygous61556001
1171539805171539806GA34GENIChomozygous61556002
1171544131171544153CACACACACACTCACAATCTCT----------------------9GENIChomozygous61556003
1171544216171544217TTCA18GENIChomozygous60942834
1171549259171549262AGA---29GENIChomozygous60942838
1171550952171550953TC28GENIChomozygous60942840
1171554726171554727GGACACAC20GENIChomozygous60942843
1171555251171555252AAAC15GENIChomozygous60942845
1171557394171557396AA--27GENIChomozygous61556006
1171558344171558345TC25GENIChomozygous61556007
1171540182171540192TGTGTGTGTG----------7GENIChomozygous62271516
1171544024171544025GGCACACACACACACA5GENICheterozygous62271517
1171560573171560574GGTGCTTGCTAGGCAAGCGCTCTACC3GENIChomozygous62173856
1171560578171560579TTGAGC4GENIChomozygous62173858
1171560614171560615CCCCCA10GENIChomozygous62173860
1171561198171561199GGGTGT8GENICheterozygous62271518
1171561324171561325TTGAGAGA14GENICheterozygous62173864
1171561324171561325TTGAGA14GENICheterozygous62271519
1171561394171561395GC22GENIChomozygous60942853
1171562104171562105TC47GENIChomozygous61556009
1171562410171562411GT23GENIChomozygous60942854
1171566604171566605GGA7GENICheterozygous60942861
1171572619171572621TT--4GENIChomozygous62271520
1171572873171572885ATACATACATAC------------23GENIChomozygous60942871
1171573027171573028TTACAC11GENICpossibly homozygous62173870
1171573994171573995TC23GENIChomozygous62271521
1171580453171580461ACACACAC--------20GENICpossibly homozygous62271522