chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117052068 117052069 A G 14 GENIC heterozygous 925281831 8 117052890 117052891 A G 27 GENIC heterozygous 925281832 8 117054122 117054123 C T 8 GENIC heterozygous 925281833 8 117054158 117054159 A G 12 GENIC heterozygous 925281834 8 117055685 117055686 C T 10 GENIC heterozygous 925281835 8 117058726 117058727 C T 27 GENIC heterozygous 925281836 8 117062340 117062341 T TGTCA 42 GENIC heterozygous 925316071 8 117065011 117065012 A G 34 GENIC heterozygous 925281837 8 117067190 117067191 G GCTGT 25 GENIC heterozygous 925316072 8 117067250 117067251 A G 29 GENIC heterozygous 925281838 8 117067587 117067588 T C 25 GENIC heterozygous 925281839 8 117068680 117068681 C A 31 GENIC heterozygous 925281840 8 117068800 117068801 A G 29 GENIC heterozygous 925281841 8 117068936 117068937 T TTC 23 GENIC heterozygous 925316073 8 117071534 117071535 C T 15 GENIC heterozygous 925281842 8 117071896 117071897 G A 13 GENIC heterozygous 925281843 8 117072006 117072007 C T 13 GENIC heterozygous 925281844 8 117072252 117072253 A AG 16 GENIC heterozygous 925316074 8 117072978 117072979 A G 29 GENIC heterozygous 925281845 8 117074996 117074997 A G 29 GENIC heterozygous 925281846