chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95697998	95698000	AC	--	6	GENIC	heterozygous	52400004
10	95699627	95699629	TG	--	13	GENIC	heterozygous	52462378
10	95701250	95701251	T	-	13	GENIC	homozygous	52683747
10	95701254	95701255	C	CAG	15	GENIC	possibly homozygous	51551996
10	95703866	95703867	G	GTATATGTGTGGTATATTAGAAGGTCTTTGTGCACTGAATATATGCATCATATTGAAAGGTGTGTGTGCAGTGTATATATGTAGCATATTCAAAGGTGTGTGTGTATGTGTGTGCAGTGTATATATGTGGTATATTCAAAGGTTGTGTGTGTGTGTCTGTGTGTCCTTGTGTGCAGTA	35	GENIC	heterozygous	52324790
10	95703912	95703913	G	GGTATATTCAAAGGTGTGTTTGTGTGTGTGTGTATGTGTGTGTGTGCAGTGTATATATGTGGTATATTCAAAGGTCTGTGTGTGTGTGTGCAGTGTATATATGTA	13	GENIC	heterozygous	52400008
10	95710791	95710793	CT	--	5	GENIC	heterozygous	52512897
10	95710836	95710837	T	-	5	GENIC	heterozygous	52604672
10	95724410	95724412	GT	--	20	GENIC	heterozygous	51552068
10	95732083	95732085	AC	--	6	GENIC	heterozygous	52400012
10	95733862	95733864	GT	--	9	GENIC	heterozygous	52400014
10	95734548	95734549	G	C	31	GENIC	homozygous	51552095
10	95734667	95734671	CCAC	----	29	GENIC	heterozygous	51552096
10	95735515	95735517	GT	--	17	GENIC	heterozygous	52651279
10	95741956	95741964	GTGTGTGT	--------	5	GENIC	heterozygous	52400016
10	95741962	95741964	GT	--	5	GENIC	heterozygous	52400018
10	95743596	95743597	T	TTG	6	GENIC	heterozygous	51998182
10	95734937	95734941	CCAT	----	11	GENIC	homozygous	52848783
10	95733858	95733864	GTGTGT	------	9	GENIC	heterozygous	52968957