chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	36095487	36095488	G	A	28	GENIC	homozygous	114313906
13	36096591	36096592	C	T	22	GENIC	homozygous	114313907
13	36096665	36096666	G	A	38	GENIC	homozygous	114313908
13	36098286	36098287	T	C	23	GENIC	homozygous	114313909
13	36099056	36099057	T	C	44	GENIC	homozygous	114313910
13	36099284	36099285	G	A	26	GENIC	homozygous	114313911
13	36099635	36099636	C	T	16	GENIC	homozygous	114313912
13	36099661	36099662	G	C	9	GENIC	homozygous	114313913
13	36099662	36099663	G	C	8	GENIC	homozygous	114313914
13	36099664	36099665	G	C	9	GENIC	homozygous	114313915
13	36099794	36099795	C	T	17	GENIC	homozygous	114313916
13	36099910	36099911	A	G	24	GENIC	homozygous	114313917
13	36100114	36100115	G	A	17	GENIC	homozygous	114313918
13	36100382	36100383	A	G	35	GENIC	homozygous	114313919
13	36100389	36100390	T	C	38	GENIC	homozygous	114313920
13	36100847	36100848	T	G	28	GENIC	homozygous	114313921
13	36101163	36101164	C	G	25	GENIC	homozygous	114313922
13	36101306	36101307	C	T	26	GENIC	homozygous	114313923
13	36097296	36097297	C	T	18	GENIC	homozygous	114528102