chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 5848891 5848892 G A 68 GENIC homozygous 782089088 14 5849304 5849305 A G 59 GENIC homozygous 782089089 14 5849445 5849446 A C 44 GENIC homozygous 782089090 14 5849476 5849477 G C 40 GENIC homozygous 782089091 14 5849630 5849631 C A 70 GENIC homozygous 782089092 14 5849751 5849752 C T 35 GENIC homozygous 782089093 14 5849782 5849783 C A 29 GENIC homozygous 782089094 14 5849838 5849839 G C 40 GENIC homozygous 782089095 14 5849853 5849854 C G 46 GENIC homozygous 782089096 14 5849872 5849873 C T 55 GENIC homozygous 782089097 14 5849885 5849886 A G 53 GENIC homozygous 782089098 14 5849909 5849910 T C 51 GENIC homozygous 782089099 14 5850030 5850031 C T 44 GENIC homozygous 782089100 14 5850239 5850240 G C 46 GENIC homozygous 782089101 14 5850522 5850523 G C 20 GENIC homozygous 782089102 14 5851682 5851683 A T 34 GENIC heterozygous 782089103 14 5851690 5851691 C T 41 GENIC heterozygous 782089104 14 5851754 5851755 C G 117 GENIC homozygous 782089105 14 5851797 5851798 T A 120 GENIC heterozygous 782089106 14 5851810 5851811 G A 121 GENIC heterozygous 782089107