chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 75196099 75196100 G - 14 GENIC homozygous 710885463 10 75197014 75197015 T C 26 GENIC homozygous 570168691 10 75197442 75197443 T C 19 GENIC homozygous 570168692 10 75198864 75198865 A G 12 GENIC homozygous 570168693 10 75201108 75201109 C T 26 GENIC homozygous 571916584 10 75201675 75201676 A - 13 GENIC homozygous 710885464 10 75206706 75206707 C CTCTCTCTCTCTCTT 7 GENIC heterozygous 710885465 10 75206729 75206737 TCTCTCTC -------- 6 GENIC homozygous 710885468 10 75206897 75206909 AGTGGCAGTGGC ------------ 6 GENIC homozygous 710885470 10 75207811 75207812 T C 3 GENIC homozygous 571916585 10 75208067 75208068 C CT 5 GENIC heterozygous 710885471 10 75208160 75208161 A G 5 GENIC homozygous 571916586 10 75208176 75208177 T C 9 GENIC homozygous 571916587 10 75209305 75209306 T C 23 GENIC homozygous 571916588 10 75210385 75210386 T C 26 GENIC homozygous 570168694 10 75210957 75210958 G C 7 GENIC homozygous 571916589 10 75211099 75211100 G A 16 GENIC homozygous 571916590 10 75211670 75211671 A AGG 4 GENIC homozygous 710885473 10 75212070 75212072 AG -- 7 GENIC homozygous 710885474 10 75212193 75212194 G A 10 GENIC homozygous 571916591 10 75212606 75212607 G T 2 GENIC homozygous 571916592 10 75212838 75212839 C CCA 6 GENIC homozygous 710885475 10 75213075 75213076 A AT 21 GENIC homozygous 710885476 10 75213092 75213093 G C 21 GENIC homozygous 570168695 10 75214050 75214051 A ATT 10 GENIC homozygous 710885477