chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578908655789094CTCTCTCT--------6GENIChomozygous722776621
135578919955789201TC--6GENICheterozygous722776623
135578922755789228TTC5GENIChomozygous722776624
135578923655789237GGTC4GENIChomozygous722776625
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC2GENIChomozygous722776626
135578942255789423CG4GENICheterozygous588682807
135578961855789622TCTC----24GENIChomozygous722776627
135578965455789656TC--26GENIChomozygous722776629
135578972455789725TTC16GENIChomozygous722776630
135578973155789732CCTCT17GENICpossibly homozygous722776631
135579103355791034GA42GENIChomozygous588552924
135579200955792010GGCA12GENICheterozygous722776632
135579200955792010GGCACA12GENICpossibly homozygous722776633
135579303055793031AG25GENIChomozygous588552925
135579307355793074T-24GENIChomozygous722776635
135579400355794004GA7GENIChomozygous588682808
135579404555794047AA--7GENICheterozygous722776636
135579446155794462CT21GENIChomozygous588552926
135579512755795128AG39GENIChomozygous588552927
135579527055795271CT26GENIChomozygous588552928
135579548355795484TC28GENIChomozygous588552929
135579568655795687GGC24GENIChomozygous722776637
135579597255795973GA34GENIChomozygous588552930
135579722655797248ACACACACACACACACACACAC----------------------11GENICheterozygous722776638
135579722855797248ACACACACACACACACACAC--------------------11GENICpossibly homozygous722776639
135579807855798079AACACC12GENICheterozygous722776641
135579807855798079AACACCC12GENICheterozygous722776643
135579808655798087AG16GENIChomozygous588682809
135579830955798310TTG20GENICpossibly homozygous722776645
135579838855798389AAGACTGACTGACTGACT24GENIChomozygous722776647
135579909955799100AC29GENIChomozygous588552931
135579987755799878AG27GENIChomozygous588552932
135580062355800624CG21GENIChomozygous588552933
135580164955801650AG27GENIChomozygous588552934
135580172555801726AG20GENIChomozygous588552935