chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 89341911 89341912 A G 16 GENIC possibly homozygous 950581954 10 89343386 89343387 A G 15 GENIC homozygous 950581955 10 89343674 89343675 C T 23 GENIC homozygous 950581956 10 89344143 89344144 A G 12 GENIC homozygous 950581957 10 89344668 89344669 G A 13 GENIC homozygous 950581958 10 89345615 89345616 G C 18 GENIC homozygous 950581959 10 89346680 89346681 C T 17 GENIC homozygous 950581960 10 89346990 89346991 T C 11 GENIC homozygous 950581961 10 89348227 89348228 A G 21 GENIC homozygous 950581962 10 89348259 89348260 C T 18 GENIC homozygous 950581963 10 89348541 89348542 G A 13 GENIC homozygous 950581964 10 89348632 89348633 G A 22 GENIC homozygous 950581965 10 89348648 89348649 C T 22 GENIC homozygous 950581966 10 89348688 89348689 T C 21 GENIC homozygous 950581967 10 89348971 89348972 A C 18 GENIC homozygous 950581968 10 89349010 89349011 G A 25 GENIC homozygous 950581969 10 89349174 89349175 T C 18 GENIC homozygous 950581970 10 89349186 89349187 C G 18 GENIC homozygous 950581971