chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4156326056156326057TC9GENIChomozygous112902727
4156327217156327218TC14GENIChomozygous112902729
4156330018156330019TG13GENIChomozygous112902735
4156330043156330044TC14GENIChomozygous112902737
4156331395156331396GT15GENIChomozygous112902743
4156334066156334067CT13GENIChomozygous112902747
4156334256156334257CG11GENIChomozygous112902749
4156338304156338305GC12GENIChomozygous112902757
4156338348156338349GT15GENIChomozygous112902759
4156339512156339513TC13GENIChomozygous112902761
4156341518156341519TC16GENIChomozygous112902771
4156343126156343127CA16GENICpossibly homozygous112902775
4156347577156347578AC13GENIChomozygous112902789
4156347657156347658AT6GENIChomozygous112902791
4156348975156348976CT11GENIChomozygous112902793
4156349719156349720TA24GENIChomozygous112902795
4156349940156349941TC19GENIChomozygous112902797
4156350864156350865CT9GENIChomozygous112902799
4156350994156350995GT12GENIChomozygous112902801
4156352059156352060AG9GENIChomozygous113062397
4156352218156352219TC5GENIChomozygous112902805
4156353473156353474CT7GENIChomozygous112902807
4156355319156355320AC9GENIChomozygous112902809
4156355820156355821AG6GENIChomozygous112902811
4156358110156358111GC10GENIChomozygous112902829