chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	38605191	38605192	C	T	16	GENIC	possibly homozygous	116925140
10	38605273	38605274	C	A	22	GENIC	homozygous	116977179
10	38609941	38609942	G	A	12	GENIC	homozygous	116925144
10	38613884	38613885	A	C	12	GENIC	homozygous	116762165
10	38615213	38615214	G	A	20	GENIC	homozygous	116925146
10	38615408	38615409	C	T	20	GENIC	possibly homozygous	117312363
10	38619381	38619382	A	G	21	GENIC	homozygous	117125942
10	38621034	38621035	T	C	15	GENIC	homozygous	116762175
10	38624238	38624239	T	C	32	GENIC	homozygous	116925152
10	38627069	38627070	C	A	13	GENIC	homozygous	117125944
10	38628270	38628271	C	T	22	GENIC	homozygous	116762181
10	38628331	38628332	G	A	19	GENIC	homozygous	116762183
10	38629567	38629568	G	A	26	GENIC	homozygous	117125946
10	38633864	38633865	G	T	11	GENIC	homozygous	117076571
10	38637471	38637472	A	G	21	GENIC	homozygous	116925154
10	38641813	38641814	C	A	21	GENIC	possibly homozygous	116977185
10	38615518	38615519	C	T	24	GENIC	homozygous	118065698
10	38623683	38623684	C	T	22	GENIC	homozygous	118065699
10	38640363	38640364	A	G	23	GENIC	homozygous	118065701
10	38640365	38640366	T	C	23	GENIC	homozygous	118065702