chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10340593	10340594	C	T	19	GENIC	homozygous	109633596
19	10341178	10341179	A	C	22	GENIC	homozygous	109633598
19	10341308	10341309	A	G	22	GENIC	homozygous	109764542
19	10342191	10342192	G	A	16	GENIC	homozygous	109633600
19	10342841	10342842	A	G	23	GENIC	homozygous	109633602
19	10342891	10342892	A	G	22	GENIC	homozygous	109633604
19	10345773	10345774	C	T	11	GENIC	homozygous	109633606
19	10345778	10345779	A	G	14	GENIC	homozygous	109633608
19	10348263	10348264	T	C	12	GENIC	homozygous	109633610
19	10349055	10349062	GGGGAGT		21	GENIC	homozygous	129583440
19	10349567	10349568	C	T	12	GENIC	homozygous	109633612
19	10350452	10350453	G	A	22	GENIC	homozygous	109633614
19	10352595	10352596	C		16	GENIC	homozygous	129583441
19	10353717	10353723	TCTCTC		16	GENIC	homozygous	129583442
19	10353725	10353725		G	16	GENIC	homozygous	129583443
19	10353726	10353726		ACATGAGC	16	GENIC	homozygous	129583444
19	10354967	10354968	T	C	20	GENIC	homozygous	109633616
19	10355021	10355022	T	C	16	GENIC	homozygous	109633618
19	10355526	10355527	G	A	15	GENIC	homozygous	109633620
19	10357629	10357630	A	G	13	GENIC	homozygous	109633622
19	10358482	10358483	C	T	9	GENIC	homozygous	109633624
19	10359004	10359005	G	T	19	GENIC	homozygous	109633626
19	10359212	10359213	A	G	11	GENIC	homozygous	109633628