chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95697036	95697040	TTTT	----	7	GENIC	heterozygous	52512895
10	95697998	95698000	AC	--	5	GENIC	heterozygous	52400004
10	95701249	95701250	C	CACA	13	GENIC	heterozygous	51551994
10	95701250	95701251	T	C	13	GENIC	heterozygous	52400006
10	95701250	95701251	T	-	13	GENIC	heterozygous	52683747
10	95701254	95701255	C	CAG	13	GENIC	heterozygous	51551996
10	95703912	95703913	G	GGTATATTCAAAGGTGTGTTTGTGTGTGTGTGTATGTGTGTGTGTGCAGTGTATATATGTGGTATATTCAAAGGTCTGTGTGTGTGTGTGCAGTGTATATATGTA	18	GENIC	heterozygous	52400008
10	95709608	95709609	G	GGT	2	GENIC	heterozygous	52604669
10	95710791	95710793	CT	--	4	GENIC	heterozygous	52512897
10	95712743	95712744	T	-	21	GENIC	heterozygous	51552031
10	95732083	95732085	AC	--	4	GENIC	heterozygous	52400012
10	95733857	95733858	G	GGT	7	GENIC	heterozygous	52810874
10	95733862	95733864	GT	--	7	GENIC	heterozygous	52400014
10	95734548	95734549	G	C	25	GENIC	homozygous	51552095
10	95734667	95734671	CCAC	----	49	GENIC	heterozygous	51552096
10	95729977	95729979	AT	--	10	GENIC	heterozygous	51750831
10	95735515	95735517	GT	--	16	GENIC	heterozygous	52651279
10	95741962	95741964	GT	--	2	GENIC	heterozygous	52400018
10	95734937	95734941	CCAT	----	28	GENIC	homozygous	52848783