chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 47904360 47904361 C T 28 GENIC homozygous 795390639 12 47904428 47904429 A G 25 GENIC homozygous 795390640 12 47905039 47905040 G C 32 GENIC homozygous 795390641 12 47905057 47905058 C T 34 GENIC homozygous 795390642 12 47905332 47905333 G A 14 GENIC homozygous 795390643 12 47905924 47905925 T C 52 GENIC homozygous 795390644 12 47906897 47906898 G A 31 GENIC possibly homozygous 795390645 12 47907186 47907187 T C 35 GENIC homozygous 795390646 12 47907234 47907235 C T 36 GENIC homozygous 795390647 12 47907550 47907551 A G 35 GENIC homozygous 795390648 12 47908074 47908075 G A 33 GENIC homozygous 795390649 12 47908182 47908183 T C 43 GENIC homozygous 795390650 12 47908531 47908532 C T 28 GENIC homozygous 795390651 12 47909783 47909784 G T 22 GENIC homozygous 795390652 12 47910882 47910883 G A 28 GENIC homozygous 795390653 12 47911032 47911033 A G 28 GENIC homozygous 795390654 12 47911186 47911187 C T 34 GENIC homozygous 795390655 12 47911268 47911269 G A 19 GENIC heterozygous 795390656 12 47912110 47912111 G A 31 GENIC homozygous 795390657 12 47912142 47912143 A G 33 GENIC homozygous 795390658 12 47912338 47912339 C T 37 GENIC homozygous 795390659 12 47912378 47912379 C T 37 GENIC homozygous 795390660 12 47912528 47912529 A G 39 GENIC homozygous 795390661 12 47913298 47913299 T C 43 GENIC homozygous 795390662 12 47913961 47913962 C A 33 GENIC homozygous 795390663 12 47913964 47913965 C A 32 GENIC homozygous 795390664 12 47914094 47914095 G A 41 GENIC homozygous 795390665 12 47914212 47914213 G A 26 GENIC homozygous 795390666 12 47915391 47915392 T C 31 GENIC homozygous 795390667 12 47917034 47917035 G A 50 GENIC homozygous 795390668 12 47917208 47917209 T C 31 GENIC homozygous 795390669 12 47918696 47918697 G C 24 GENIC heterozygous 795390670 12 47918708 47918709 G C 21 GENIC possibly homozygous 795390671 12 47919368 47919369 T C 47 GENIC homozygous 795390672 12 47919858 47919859 A C 36 GENIC homozygous 795390673