chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104726060	104726063	TCC	---	24	INTERGENIC	heterozygous	52404460
10	104726064	104726073	GTGGCACCG	---------	27	INTERGENIC	heterozygous	52404462
10	104726211	104726212	A	AGG	28	INTERGENIC	heterozygous	52404464
10	104727548	104727555	CAAAGTC	-------	30	INTERGENIC	homozygous	51589476
10	104728091	104728092	T	TTATTGGC	31	INTERGENIC	homozygous	51589478
10	104743138	104743139	C	G	11	GENIC	homozygous	51589486
10	104743140	104743141	A	G	11	GENIC	homozygous	51589488
10	104743326	104743327	A	G	24	GENIC	homozygous	51589490
10	104743330	104743331	A	G	24	GENIC	homozygous	51589492
10	104743332	104743333	A	T	23	GENIC	homozygous	51589494
10	104743344	104743345	A	G	23	GENIC	homozygous	51589496
10	104743347	104743348	C	G	24	GENIC	homozygous	51589498
10	104743356	104743357	A	G	23	GENIC	homozygous	51589500
10	104743360	104743361	A	G	24	GENIC	homozygous	51589502
10	104743362	104743363	G	T	24	GENIC	homozygous	51589504
10	104743390	104743391	G	-	17	GENIC	homozygous	51589506
10	104743406	104743407	A	G	14	GENIC	homozygous	51589509
10	104743503	104743504	A	-	23	GENIC	homozygous	51589511
10	104743600	104743601	G	-	19	GENIC	homozygous	51589513
10	104743612	104743613	T	-	17	GENIC	homozygous	51589515
10	104743652	104743653	G	-	27	GENIC	homozygous	51589517
10	104743661	104743662	G	-	30	GENIC	homozygous	51589519
10	104743856	104743857	G	GC	13	GENIC	homozygous	51589521
10	104743871	104743872	G	GC	8	GENIC	homozygous	51589523
10	104745121	104745122	G	GA	2	GENIC	heterozygous	52404466