chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	43405296	43405297	C	T	36	GENIC	heterozygous	112271565
3	43405316	43405317	C	T	32	GENIC	heterozygous	112271566
3	43405334	43405335	A	C	28	GENIC	heterozygous	112271567
3	43405335	43405336	A	G	28	GENIC	heterozygous	112271568
3	43405339	43405340	G	C	27	GENIC	heterozygous	112271569
3	43405352	43405353	A	C	40	GENIC	heterozygous	112271570
3	43405357	43405358	A	G	43	GENIC	heterozygous	112271571
3	43405363	43405364	C	T	46	GENIC	heterozygous	112271572
3	43405370	43405371	T	C	45	GENIC	heterozygous	112271573
3	43405376	43405377	G	C	43	GENIC	heterozygous	112271574
3	43405381	43405382	C	G	46	GENIC	heterozygous	112271575
3	43408702	43408703	G	A	13	GENIC	possibly homozygous	111550775
3	43408708	43408709	A	G	17	GENIC	homozygous	111550776
3	43414454	43414455	G	A	10	GENIC	homozygous	111550780
3	43414524	43414525	T	G	59	GENIC	possibly homozygous	111550781
3	43414582	43414583	T	A	46	GENIC	homozygous	111550782
3	43414692	43414693	A	G	27	GENIC	homozygous	111550783
3	43414733	43414734	C	G	19	GENIC	homozygous	111550784
3	43417581	43417582	C	A	38	GENIC	heterozygous	111904351
3	43417737	43417738	A	G	98	GENIC	heterozygous	111550787
3	43417981	43417982	C	T	64	GENIC	heterozygous	112271576
3	43420327	43420328	T	G	26	GENIC	homozygous	111550790
3	43420371	43420372	C	G	15	GENIC	homozygous	111550792
3	43420396	43420397	T	C	15	GENIC	homozygous	111550793
3	43421145	43421146	T	C	12	GENIC	homozygous	111904353