chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	107339039	107339040	T	C	18	GENIC	possibly homozygous	51592760
10	107340451	107340452	A	C	17	GENIC	homozygous	51592764
10	107341324	107341325	T	C	23	GENIC	homozygous	51592766
10	107341590	107341591	A	G	11	GENIC	homozygous	51592768
10	107341880	107341881	A	G	23	GENIC	possibly homozygous	51592770
10	107342063	107342064	G	A	22	GENIC	homozygous	51592772
10	107342549	107342550	A	G	22	GENIC	possibly homozygous	51592774
10	107343707	107343708	T	C	33	GENIC	homozygous	51592776
10	107343993	107343994	T	G	9	GENIC	possibly homozygous	51592778
10	107344260	107344261	A	G	23	GENIC	homozygous	51592780
10	107344886	107344887	C	T	18	GENIC	possibly homozygous	51592782
10	107345329	107345330	C	G	19	GENIC	homozygous	51592784
10	107345395	107345396	C	CT	7	GENIC	heterozygous	51592786
10	107350988	107350989	C	T	5	GENIC	homozygous	51592792
10	107355198	107355199	C	-	27	GENIC	heterozygous	51592794
10	107357217	107357218	C	A	19	GENIC	homozygous	51592796
10	107357560	107357561	A	AC	4	GENIC	homozygous	51592802
10	107359298	107359299	T	G	18	GENIC	possibly homozygous	51592806
10	107364435	107364436	C	G	5	GENIC	heterozygous	51592810
10	107364606	107364607	A	AG	2	GENIC	homozygous	51592812
10	107371570	107371590	AGGTGTGGCCTTGTTGGAAT	--------------------	12	GENIC	heterozygous	52575995
10	107372965	107372966	C	T	19	GENIC	possibly homozygous	51592824
10	107374810	107374811	T	C	21	GENIC	homozygous	51592828
10	107379981	107379982	C	CAG	7	GENIC	heterozygous	51592840
10	107380213	107380214	C	T	22	GENIC	homozygous	51592844
10	107380389	107380390	C	-	3	GENIC	heterozygous	51592846
10	107380967	107380968	T	TG	15	GENIC	possibly homozygous	51592852
10	107381968	107381969	G	A	11	GENIC	homozygous	51592854
10	107382307	107382308	C	T	16	GENIC	heterozygous	51592856
10	107382621	107382622	C	T	23	GENIC	homozygous	51592858
10	107383007	107383008	C	G	17	GENIC	homozygous	51592860
10	107383410	107383411	G	A	15	GENIC	possibly homozygous	51592862
10	107384091	107384092	T	C	20	GENIC	possibly homozygous	51592864
10	107384120	107384121	C	G	19	GENIC	possibly homozygous	51592866
10	107385537	107385539	GT	--	8	GENIC	possibly homozygous	51592868