chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 32194000 32194001 C T 1 GENIC homozygous 548577905 7 32195369 32195370 C T 10 GENIC possibly homozygous 548577906 7 32195539 32195540 C T 9 GENIC heterozygous 548577907 7 32195567 32195568 T C 18 GENIC possibly homozygous 548577908 7 32195662 32195663 T C 8 GENIC homozygous 548577909 7 32195765 32195766 G A 11 GENIC homozygous 548577910 7 32195866 32195867 C G 8 GENIC homozygous 548577911 7 32195925 32195926 T TCAG 3 GENIC homozygous 699046006 7 32196031 32196032 C T 13 GENIC homozygous 548577912 7 32198248 32198249 T A 1 GENIC homozygous 548577913 7 32198272 32198273 T A 8 GENIC homozygous 548577914 7 32198291 32198292 C A 8 GENIC homozygous 548577915 7 32198378 32198379 T A 3 GENIC homozygous 547303565 7 32200007 32200008 C T 21 GENIC possibly homozygous 548577916 7 32200326 32200327 A G 16 GENIC homozygous 548577917 7 32200367 32200368 T C 19 GENIC homozygous 548577918 7 32219183 32219184 T C 11 GENIC homozygous 547303566 7 32224258 32224259 G A 24 GENIC homozygous 548577919 7 32225388 32225389 A G 14 GENIC possibly homozygous 548577920 7 32225399 32225400 T C 11 GENIC homozygous 548577921 7 32225418 32225419 C T 16 GENIC homozygous 548577922 7 32225558 32225559 G C 24 GENIC homozygous 548577923