chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 47067387 47067388 T C 27 GENIC homozygous 997898611 10 47068507 47068508 A G 24 GENIC homozygous 997898612 10 47081680 47081681 C T 33 GENIC homozygous 997898613 10 47082373 47082374 G A 21 GENIC homozygous 997898614 10 47083081 47083082 G A 35 GENIC homozygous 997898615 10 47083672 47083673 T C 29 GENIC homozygous 997898616 10 47084322 47084323 A G 30 GENIC homozygous 997898617 10 47084461 47084462 T C 21 GENIC homozygous 997898618 10 47085873 47085874 T C 21 GENIC homozygous 997898619 10 47086422 47086423 G C 25 GENIC possibly homozygous 997898620 10 47086500 47086501 A G 43 GENIC homozygous 997898621 10 47086652 47086653 C A 26 GENIC homozygous 997898622 10 47087348 47087349 G A 30 GENIC homozygous 997898623 10 47089091 47089092 G T 37 GENIC homozygous 997898624 10 47089961 47089962 T C 16 GENIC homozygous 997898625 10 47091233 47091234 G A 28 GENIC homozygous 997898626 10 47091288 47091289 G T 30 GENIC homozygous 997898627 10 47091533 47091534 C T 30 GENIC homozygous 997898628 10 47092963 47092964 T C 20 GENIC homozygous 997898629 10 47093708 47093709 T C 16 GENIC homozygous 997898630 10 47093872 47093873 G C 15 GENIC homozygous 997898631 10 47093905 47093906 T A 17 GENIC homozygous 997898632 10 47095400 47095401 A C 16 GENIC homozygous 997898633 10 47096988 47096989 C T 44 GENIC homozygous 997898634 10 47097004 47097005 T C 42 GENIC homozygous 997898635 10 47097812 47097813 T C 17 GENIC homozygous 997898636 10 47098398 47098399 C T 25 GENIC homozygous 997898637 10 47101758 47101759 C T 37 GENIC homozygous 997898638