chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95697036	95697040	TTTT	----	5	GENIC	heterozygous	52512895
10	95697997	95697998	A	AAC	9	GENIC	heterozygous	51551979
10	95697998	95698000	AC	--	9	GENIC	heterozygous	52400004
10	95701249	95701250	C	CACA	14	GENIC	homozygous	51551994
10	95701250	95701251	T	C	14	GENIC	homozygous	52400006
10	95703866	95703867	G	GTATATGTGTGGTATATTAGAAGGTCTTTGTGCACTGAATATATGCATCATATTGAAAGGTGTGTGTGCAGTGTATATATGTAGCATATTCAAAGGTGTGTGTGTATGTGTGTGCAGTGTATATATGTGGTATATTCAAAGGTTGTGTGTGTGTGTCTGTGTGTCCTTGTGTGCAGTA	48	GENIC	heterozygous	52324790
10	95703912	95703913	G	GGTATATTCAAAGGTGTGTTTGTGTGTGTGTGTATGTGTGTGTGTGCAGTGTATATATGTGGTATATTCAAAGGTCTGTGTGTGTGTGTGCAGTGTATATATGTA	24	GENIC	heterozygous	52400008
10	95710791	95710793	CT	--	5	GENIC	heterozygous	52512897
10	95716375	95716377	GT	--	8	GENIC	heterozygous	51750828
10	95718080	95718082	GT	--	15	GENIC	heterozygous	52462379
10	95724410	95724412	GT	--	7	GENIC	heterozygous	51552068
10	95734548	95734549	G	C	29	GENIC	homozygous	51552095
10	95734667	95734671	CCAC	----	52	GENIC	heterozygous	51552096
10	95741956	95741964	GTGTGTGT	--------	10	GENIC	heterozygous	52400016
10	95741962	95741964	GT	--	10	GENIC	heterozygous	52400018
10	95743596	95743597	T	TTG	5	GENIC	homozygous	51998182