chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 79181991 79181992 G A 25 GENIC homozygous 108873838 1 79182107 79182108 C A 8 GENIC homozygous 108873839 1 79182347 79182348 G T 27 GENIC homozygous 108873840 1 79182450 79182451 T C 38 GENIC homozygous 108873841 1 79182938 79182939 G A 24 GENIC homozygous 108873842 1 79184791 79184792 T C 30 GENIC homozygous 108873843 1 79184818 79184819 T A 38 GENIC homozygous 108873844 1 79185160 79185161 C G 21 GENIC homozygous 108873845 1 79185391 79185392 T A 21 GENIC homozygous 108873846 1 79185421 79185422 T C 18 GENIC homozygous 108873847 1 79185529 79185530 T C 24 GENIC homozygous 108873848 1 79185698 79185699 C T 23 GENIC homozygous 108873849 1 79186037 79186038 T C 37 GENIC homozygous 108873850 1 79186228 79186229 C T 23 GENIC homozygous 108873851 1 79186871 79186872 T C 21 GENIC homozygous 108873852 1 79187493 79187494 T C 31 GENIC homozygous 108873853 1 79187865 79187866 G C 20 GENIC homozygous 108873854 1 79188030 79188031 A G 22 GENIC homozygous 108873855 1 79188353 79188354 C T 25 GENIC homozygous 108873856 1 79188871 79188872 A T 31 GENIC homozygous 108873857 1 79188985 79188986 C T 28 GENIC homozygous 108873858 1 79188988 79188989 C T 28 GENIC homozygous 108873859 1 79190631 79190632 G A 21 GENIC homozygous 108873860