chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 47067387 47067388 T C 26 GENIC homozygous 976552609 10 47068507 47068508 A G 21 GENIC homozygous 976552610 10 47082373 47082374 G A 23 GENIC homozygous 976552611 10 47083081 47083082 G A 18 GENIC homozygous 976552612 10 47083672 47083673 T C 25 GENIC homozygous 976552613 10 47084322 47084323 A G 25 GENIC homozygous 976552614 10 47084461 47084462 T C 21 GENIC homozygous 976552615 10 47086422 47086423 G C 35 GENIC homozygous 976552616 10 47086500 47086501 A G 26 GENIC homozygous 976552617 10 47086652 47086653 C A 31 GENIC homozygous 976552618 10 47087348 47087349 G A 35 GENIC homozygous 976552619 10 47087639 47087640 C T 14 GENIC homozygous 976552620 10 47088193 47088194 G T 23 GENIC homozygous 976552621 10 47089091 47089092 G T 25 GENIC homozygous 976552622 10 47089961 47089962 T C 16 GENIC homozygous 976552623 10 47090095 47090096 T A 10 GENIC homozygous 976552624 10 47091233 47091234 G A 29 GENIC homozygous 976552625 10 47091288 47091289 G T 20 GENIC homozygous 976552626 10 47091533 47091534 C T 26 GENIC homozygous 976552627 10 47092963 47092964 T C 21 GENIC homozygous 976552628 10 47093708 47093709 T C 30 GENIC homozygous 976552629 10 47093905 47093906 T A 24 GENIC homozygous 976552630 10 47094019 47094020 T C 23 GENIC homozygous 976552631 10 47095400 47095401 A C 14 GENIC homozygous 976552632 10 47096988 47096989 C T 17 GENIC homozygous 976552633 10 47097004 47097005 T C 15 GENIC homozygous 976552634 10 47097812 47097813 T C 17 GENIC homozygous 976552635 10 47098398 47098399 C T 21 GENIC homozygous 976552636 10 47101758 47101759 C T 18 GENIC homozygous 976552637