chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 5848891 5848892 G A 36 GENIC possibly homozygous 777063671 14 5849304 5849305 A G 44 GENIC homozygous 777063672 14 5849445 5849446 A C 45 GENIC homozygous 777063673 14 5849476 5849477 G C 35 GENIC homozygous 777063674 14 5849630 5849631 C A 43 GENIC homozygous 777063675 14 5849751 5849752 C T 45 GENIC homozygous 777063676 14 5849853 5849854 C G 48 GENIC homozygous 777063677 14 5849872 5849873 C T 49 GENIC homozygous 777063678 14 5849885 5849886 A G 44 GENIC homozygous 777063679 14 5849909 5849910 T C 51 GENIC homozygous 777063680 14 5850030 5850031 C T 52 GENIC homozygous 777063681 14 5850239 5850240 G C 56 GENIC homozygous 777063682 14 5850522 5850523 G C 17 GENIC homozygous 777063683 14 5851611 5851612 G A 31 GENIC homozygous 777063684 14 5851616 5851617 C T 32 GENIC homozygous 777063685 14 5851648 5851649 C T 40 GENIC heterozygous 777063686 14 5851682 5851683 A T 55 GENIC heterozygous 777063687 14 5851690 5851691 C T 61 GENIC heterozygous 777063688 14 5851754 5851755 C G 124 GENIC homozygous 777063689