chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104726163	104726164	T	C	20	INTERGENIC	heterozygous	51589472
10	104726173	104726174	G	A	19	INTERGENIC	heterozygous	51589474
10	104727548	104727555	CAAAGTC	-------	16	INTERGENIC	homozygous	51589476
10	104728091	104728092	T	TTATTGGC	10	INTERGENIC	homozygous	51589478
10	104743326	104743327	A	G	8	GENIC	homozygous	51589490
10	104743330	104743331	A	G	7	GENIC	homozygous	51589492
10	104743332	104743333	A	T	7	GENIC	homozygous	51589494
10	104743344	104743345	A	G	8	GENIC	homozygous	51589496
10	104743347	104743348	C	G	8	GENIC	homozygous	51589498
10	104743356	104743357	A	G	7	GENIC	homozygous	51589500
10	104743360	104743361	A	G	7	GENIC	homozygous	51589502
10	104743362	104743363	G	T	7	GENIC	homozygous	51589504
10	104743390	104743391	G	-	10	GENIC	homozygous	51589506
10	104743406	104743407	A	G	10	GENIC	homozygous	51589509
10	104743503	104743504	A	-	11	GENIC	homozygous	51589511
10	104743600	104743601	G	-	8	GENIC	homozygous	51589513
10	104743612	104743613	T	-	9	GENIC	homozygous	51589515
10	104743652	104743653	G	-	6	GENIC	homozygous	51589517
10	104743661	104743662	G	-	8	GENIC	homozygous	51589519
10	104743856	104743857	G	GC	11	GENIC	homozygous	51589521
10	104743871	104743872	G	GC	7	GENIC	homozygous	51589523