chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	170354258	170354259	C	T	36	GENIC	homozygous	111834318
3	170356262	170356263	A	T	24	GENIC	homozygous	111834320
3	170356401	170356402	A	T	47	GENIC	homozygous	111834322
3	170356511	170356512	C	T	9	GENIC	possibly homozygous	111834324
3	170357958	170357959	G	A	73	GENIC	homozygous	111834326
3	170358050	170358051	T	G	57	GENIC	homozygous	111834328
3	170358205	170358206	C	T	55	GENIC	homozygous	111834330
3	170358303	170358304	G	T	40	GENIC	homozygous	111834332
3	170358311	170358312	G	A	41	GENIC	possibly homozygous	111834334
3	170358446	170358447	A	G	16	GENIC	homozygous	112046991
3	170358743	170358744	T	C	39	GENIC	homozygous	111834336
3	170359093	170359094	G	A	47	GENIC	homozygous	111834338
3	170359350	170359351	C	T	60	GENIC	homozygous	111834340
3	170360663	170360664	C	A	47	GENIC	homozygous	111834342
3	170360792	170360793	G	C	76	GENIC	homozygous	111834344
3	170361906	170361907	G	T	44	GENIC	possibly homozygous	111834346
3	170362065	170362066	A	G	56	GENIC	homozygous	111834348
3	170362161	170362162	G	A	50	GENIC	homozygous	111834350
3	170363076	170363077	G	A	54	GENIC	homozygous	111834352