chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117052068 117052069 A G 14 GENIC heterozygous 925462831 8 117052890 117052891 A G 28 GENIC heterozygous 925462832 8 117054122 117054123 C T 16 GENIC heterozygous 925462833 8 117054158 117054159 A G 13 GENIC heterozygous 925462834 8 117055685 117055686 C T 12 GENIC heterozygous 925462835 8 117058726 117058727 C T 77 GENIC heterozygous 925462836 8 117062340 117062341 T TGTCA 55 GENIC heterozygous 925494839 8 117065011 117065012 A G 32 GENIC heterozygous 925462837 8 117066348 117066349 C T 15 GENIC heterozygous 925462838 8 117066426 117066427 G A 8 GENIC heterozygous 925462839 8 117067190 117067191 G GCTGT 29 GENIC heterozygous 925494840 8 117067250 117067251 A G 24 GENIC heterozygous 925462840 8 117067587 117067588 T C 33 GENIC heterozygous 925462841 8 117068680 117068681 C A 42 GENIC heterozygous 925462842 8 117068800 117068801 A G 30 GENIC heterozygous 925462843 8 117068936 117068937 T TTC 28 GENIC heterozygous 925494841 8 117071534 117071535 C T 15 GENIC heterozygous 925462844 8 117071896 117071897 G A 18 GENIC heterozygous 925462845 8 117072006 117072007 C T 16 GENIC heterozygous 925462846 8 117072252 117072253 A AG 10 GENIC heterozygous 925494842 8 117072978 117072979 A G 23 GENIC heterozygous 925462847 8 117074996 117074997 A G 38 GENIC heterozygous 925462848 8 117075165 117075166 A G 15 GENIC heterozygous 925462849