chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	153102863	153102864	C	A	27	GENIC	homozygous	112042585
3	153104481	153104482	A	G	26	GENIC	homozygous	112042586
3	153105111	153105112	T	C	10	GENIC	homozygous	112042589
3	153105995	153105996	C	A	35	GENIC	homozygous	112042591
3	153106414	153106415	G	A	27	GENIC	homozygous	112042592
3	153106611	153106612	A	G	34	GENIC	homozygous	112042593
3	153106651	153106652	T	G	33	GENIC	homozygous	112042594
3	153106715	153106716	C	T	30	GENIC	homozygous	112042595
3	153106870	153106871	A	C	32	GENIC	homozygous	112042596
3	153107297	153107298	A	C	28	GENIC	homozygous	112042598
3	153108011	153108012	T	C	24	GENIC	homozygous	112042600
3	153110276	153110277	C	A	17	GENIC	homozygous	112042601
3	153110645	153110646	C	T	16	GENIC	homozygous	112042602
3	153110952	153110953	A	G	19	GENIC	homozygous	112042603
3	153111342	153111343	A	G	19	GENIC	possibly homozygous	112042604
3	153111884	153111885	T	C	22	GENIC	homozygous	112042605
3	153111936	153111937	C	T	19	GENIC	homozygous	112042606
3	153112318	153112319	C	T	25	GENIC	homozygous	112042607
3	153114684	153114685	T	C	19	GENIC	homozygous	112042608