chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	153449331	153449332	G	A	18	GENIC	homozygous	125940616
3	153449459	153449460	G	A	30	GENIC	homozygous	125940617
3	153452444	153452445	C	T	26	GENIC	homozygous	125940618
3	153453071	153453072	A	G	15	GENIC	homozygous	112043316
3	153451087	153451088	A	G	27	GENIC	homozygous	112043312
3	153453777	153453778	C	T	26	GENIC	homozygous	125940619
3	153454314	153454315	G	A	24	GENIC	homozygous	125940620
3	153454614	153454615	T	C	22	GENIC	homozygous	112043321
3	153455021	153455022	C	T	26	GENIC	homozygous	125940621
3	153455417	153455418	G	A	24	GENIC	possibly homozygous	125940622
3	153456018	153456019	G	A	21	GENIC	homozygous	125940623
3	153457002	153457003	A	G	29	GENIC	homozygous	112043328
3	153457474	153457475	C	T	12	GENIC	possibly homozygous	125940624
3	153458596	153458597	A	T	17	GENIC	homozygous	112043334
3	153458961	153458962	T	C	24	GENIC	homozygous	112043336
3	153458964	153458966	CA		24	GENIC	homozygous	131330995
3	153460299	153460300	C	T	18	GENIC	homozygous	125940625
3	153460308	153460309	A	G	23	GENIC	homozygous	112043344
3	153460836	153460837	A	G	20	GENIC	homozygous	125940626
3	153462372	153462373	C	T	27	GENIC	homozygous	112043354
3	153464306	153464307	G	A	16	GENIC	homozygous	125940627
3	153467104	153467105	T	C	22	GENIC	homozygous	112043356
3	153457911	153457911		T	27	GENIC	homozygous	134526300