chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 71398455 71398456 T C 12 GENIC possibly homozygous 50821818 11 71399510 71399511 C G 14 GENIC heterozygous 50821820 11 71402357 71402358 G A 14 GENIC possibly homozygous 50961459 11 71402807 71402808 C T 20 GENIC possibly homozygous 50891669 11 71404779 71404780 T - 8 GENIC possibly homozygous 50961460 11 71404983 71404984 A G 16 GENIC possibly homozygous 50961461 11 71406320 71406321 T A 4 GENIC homozygous 50821831 11 71406361 71406362 T C 13 GENIC homozygous 50992404 11 71407613 71407614 G C 21 GENIC possibly homozygous 50992405 11 71409420 71409421 G T 15 GENIC homozygous 50992406 11 71409474 71409475 T - 5 GENIC heterozygous 50992407 11 71409476 71409477 T - 5 GENIC heterozygous 50992408 11 71409874 71409875 C G 22 GENIC homozygous 50992409 11 71411724 71411725 C T 17 GENIC possibly homozygous 50821836 11 71414258 71414259 T C 7 GENIC heterozygous 50961463 11 71414997 71414998 G GTC 3 GENIC homozygous 50961464 11 71415288 71415289 C T 15 GENIC homozygous 50961465 11 71415300 71415301 A G 16 GENIC possibly homozygous 50821843 11 71415598 71415599 T C 15 GENIC homozygous 50821845 11 71417959 71417960 T - 5 GENIC homozygous 50961467 11 71418214 71418215 C T 15 GENIC possibly homozygous 50891693 11 71418729 71418730 T A 16 GENIC possibly homozygous 50961468