chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13091642 13091643 A G 38 GENIC homozygous 115259742 12 13092299 13092300 G T 20 GENIC homozygous 115259744 12 13092512 13092513 G A 20 GENIC homozygous 115259746 12 13092755 13092756 T A 34 GENIC homozygous 115259748 12 13096700 13096701 G A 26 GENIC homozygous 115259750 12 13098210 13098211 G C 24 GENIC homozygous 115259752 12 13099650 13099651 T C 10 GENIC homozygous 115259754 12 13102473 13102474 T C 24 GENIC homozygous 115259756 12 13103676 13103677 C T 34 GENIC homozygous 115259758 12 13103844 13103845 A T 13 GENIC homozygous 115259760 12 13104281 13104282 G A 42 GENIC homozygous 115259762 12 13105348 13105349 C T 29 GENIC homozygous 115416645 12 13105565 13105566 T G 32 GENIC homozygous 115259764 12 13105707 13105708 C G 24 GENIC homozygous 115259766 12 13107182 13107183 C T 40 GENIC homozygous 115259768 12 13107640 13107641 C T 24 GENIC homozygous 115259770 12 13109211 13109212 C T 21 GENIC homozygous 115259772 12 13109316 13109317 G A 25 GENIC homozygous 115259774 12 13110695 13110696 T C 41 GENIC homozygous 115259776