chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106075965	106075966	T	C	19	GENIC	homozygous	117032343
10	106078288	106078289	C	T	12	GENIC	homozygous	117261123
10	106079074	106079075	A	T	35	GENIC	homozygous	117032345
10	106080278	106080279	T	G	16	GENIC	homozygous	116838858
10	106082191	106082192	T	G	20	GENIC	homozygous	117032347
10	106084288	106084289	A	G	29	GENIC	homozygous	116838862
10	106086689	106086690	A	G	22	GENIC	homozygous	117032353
10	106087974	106087975	T	C	31	GENIC	homozygous	116838872
10	106089786	106089787	G	A	12	GENIC	homozygous	117261127
10	106092267	106092268	C	T	17	GENIC	homozygous	117032355
10	106093092	106093093	A	G	15	GENIC	homozygous	116838884
10	106093780	106093781	G	T	18	GENIC	homozygous	116838886
10	106109691	106109692	G	A	15	GENIC	homozygous	117032359