chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	70433492	70433493	T	C	30	GENIC	homozygous	64259284
18	70435920	70435921	G	A	26	GENIC	homozygous	64259285
18	70436290	70436291	T	C	24	GENIC	homozygous	64259286
18	70439176	70439177	A	G	29	GENIC	homozygous	64259287
18	70441715	70441716	T	C	27	GENIC	homozygous	64259288
18	70443328	70443329	T	C	19	GENIC	homozygous	64259289
18	70444649	70444650	C	T	15	GENIC	homozygous	64259290
18	70445218	70445219	G	A	34	GENIC	homozygous	64259291
18	70445626	70445627	G	A	25	GENIC	homozygous	64259292
18	70445709	70445710	G	A	23	GENIC	possibly homozygous	64259293
18	70446055	70446056	C	T	42	GENIC	homozygous	64259294
18	70446342	70446343	T	G	14	GENIC	homozygous	64259296
18	70447948	70447949	C	T	33	GENIC	homozygous	64528439
18	70449018	70449019	C	T	33	GENIC	homozygous	64528442
18	70453075	70453076	A	G	42	GENIC	homozygous	64259297
18	70455179	70455180	A	C	30	GENIC	homozygous	64259298
18	70456127	70456128	A	C	25	GENIC	homozygous	64259299
18	70457832	70457833	C	T	22	GENIC	homozygous	64259300
18	70458082	70458083	T	C	30	GENIC	homozygous	64259301
18	70458134	70458135	A	G	35	GENIC	homozygous	64259302