chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16311939763119398CG11GENICpossibly homozygous62076441
16311977463119775CT17GENICpossibly homozygous62076442
16311981063119811AC19GENICpossibly homozygous62076443
16311991363119916TTA---21GENICpossibly homozygous62717110
16311999963120000TC24GENICpossibly homozygous62076444
16312001563120016TC24GENICpossibly homozygous62076445
16312029663120297CT29GENIChomozygous62076446
16312045063120451CA17GENIChomozygous62076447
16312052863120529CA29GENIChomozygous61704126
16312084763120848TC12GENIChomozygous62076448
16312086563120866GC17GENIChomozygous62076449
16312107363121074AT21GENIChomozygous61871809
16312112163121122CT26GENIChomozygous61871810
16312123363121234AC28GENIChomozygous61871811
16312126763121268TG31GENIChomozygous61871812
16312133863121339TC29GENIChomozygous61871813
16312199863121999CT17GENICpossibly homozygous61871814
16312262063122621AAG26GENIChomozygous61871815
16312276663122767TTTA33GENICpossibly homozygous61871816
16312277663122777TC30GENICpossibly homozygous61871817
16312322763123228GA13GENIChomozygous61871818
16312383263123833TC34GENICpossibly homozygous61871819
16312400463124005GA24GENICpossibly homozygous61871820