chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 55954267 55954268 C T 49 GENIC homozygous 783085480 19 55954280 55954281 T C 45 GENIC homozygous 783085481 19 55954436 55954437 T G 47 GENIC possibly homozygous 783085482 19 55955492 55955493 C T 38 GENIC homozygous 783085483 19 55955630 55955631 G A 30 GENIC homozygous 783085484 19 55956322 55956323 C T 61 GENIC homozygous 783085485 19 55956368 55956369 A G 60 GENIC homozygous 783085486 19 55956409 55956410 T C 63 GENIC homozygous 783085487 19 55956610 55956611 A G 28 GENIC homozygous 783085488 19 55957368 55957369 A G 57 GENIC homozygous 783085489 19 55959036 55959037 C A 62 GENIC possibly homozygous 783085490 19 55962251 55962252 T C 45 GENIC homozygous 783085491 19 55962792 55962793 G A 38 GENIC homozygous 783085492 19 55962793 55962794 T C 38 GENIC possibly homozygous 783085493 19 55962798 55962799 G A 40 GENIC possibly homozygous 783085494 19 55969496 55969497 A C 89 GENIC homozygous 783085495 19 55969634 55969635 T C 54 GENIC heterozygous 783085496 19 55969660 55969661 A T 61 GENIC heterozygous 783085497 19 55969684 55969685 A G 60 GENIC heterozygous 783085498 19 55969722 55969723 C T 51 GENIC possibly homozygous 783085499 19 55970589 55970590 A T 56 GENIC homozygous 783085500 19 55970590 55970591 A G 56 GENIC homozygous 783085501 19 55970894 55970895 G A 53 GENIC possibly homozygous 783085502 19 55971021 55971022 C T 39 GENIC homozygous 783085503 19 55971676 55971677 A G 53 GENIC homozygous 783085504 19 55972186 55972187 G C 61 GENIC possibly homozygous 783085505 19 55973010 55973011 C T 76 GENIC possibly homozygous 783085506 19 55973098 55973099 T G 82 GENIC heterozygous 783085507 19 55973747 55973748 C T 46 GENIC homozygous 783085508 19 55973754 55973755 G A 42 GENIC homozygous 783085509 19 55974009 55974010 A G 57 GENIC homozygous 783085510 19 55977203 55977204 T C 66 GENIC homozygous 783085511