chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 75196099 75196100 G - 34 GENIC homozygous 699469732 10 75197014 75197015 T C 29 GENIC homozygous 550249951 10 75197442 75197443 T C 17 GENIC homozygous 550249952 10 75198864 75198865 A G 26 GENIC homozygous 550249953 10 75201108 75201109 C T 18 GENIC homozygous 552035736 10 75201675 75201676 A - 6 GENIC heterozygous 699469733 10 75206706 75206707 C CTCTCTCTCTCTCTT 17 GENIC heterozygous 699469734 10 75206729 75206737 TCTCTCTC -------- 4 GENIC homozygous 699469737 10 75206897 75206909 AGTGGCAGTGGC ------------ 22 GENIC homozygous 699469739 10 75207811 75207812 T C 29 GENIC homozygous 552035737 10 75208067 75208068 C CT 12 GENIC heterozygous 699469740 10 75208160 75208161 A G 27 GENIC homozygous 552035738 10 75208176 75208177 T C 34 GENIC homozygous 552035739 10 75209305 75209306 T C 40 GENIC homozygous 552035740 10 75210385 75210386 T C 37 GENIC homozygous 550249954 10 75210957 75210958 G C 24 GENIC homozygous 552035741 10 75211099 75211100 G A 31 GENIC homozygous 552035742 10 75211670 75211671 A AG 10 GENIC heterozygous 699469741 10 75211670 75211671 A AGG 10 GENIC possibly homozygous 699469742 10 75212070 75212072 AG -- 36 GENIC homozygous 699469743 10 75212193 75212194 G A 29 GENIC homozygous 552035743 10 75212606 75212607 G T 8 GENIC homozygous 552035744 10 75212838 75212839 C CCA 26 GENIC homozygous 699469744 10 75213075 75213076 A AT 23 GENIC homozygous 699469745 10 75213092 75213093 G C 21 GENIC homozygous 550249955 10 75214050 75214051 A ATT 26 GENIC possibly homozygous 699469746