chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117052068 117052069 A G 9 GENIC heterozygous 925102226 8 117052890 117052891 A G 19 GENIC heterozygous 925102227 8 117054122 117054123 C T 15 GENIC heterozygous 925102228 8 117054158 117054159 A G 12 GENIC heterozygous 925102229 8 117055685 117055686 C T 10 GENIC heterozygous 925102230 8 117058726 117058727 C T 28 GENIC heterozygous 925102231 8 117062340 117062341 T TGTCA 40 GENIC heterozygous 925133798 8 117065011 117065012 A G 38 GENIC heterozygous 925102232 8 117067190 117067191 G GCTGT 25 GENIC heterozygous 925133799 8 117067250 117067251 A G 21 GENIC heterozygous 925102233 8 117067587 117067588 T C 23 GENIC heterozygous 925102234 8 117068680 117068681 C A 35 GENIC heterozygous 925102235 8 117068800 117068801 A G 27 GENIC heterozygous 925102236 8 117068936 117068937 T TTC 13 GENIC heterozygous 925133800 8 117071534 117071535 C T 12 GENIC heterozygous 925102237 8 117072006 117072007 C T 18 GENIC heterozygous 925102238 8 117072252 117072253 A AG 12 GENIC heterozygous 925133801 8 117072978 117072979 A G 13 GENIC heterozygous 925102239 8 117074996 117074997 A G 33 GENIC heterozygous 925102240 8 117075165 117075166 A G 14 GENIC heterozygous 925102241