chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94642475	94642476	T	C	19	GENIC	homozygous	138854774
10	94650598	94650599	C	T	23	GENIC	homozygous	138854789
10	94646001	94646001		CTCTCTCTCTCTCTCTCTCTC	10	GENIC	heterozygous	148544418
10	94646002	94646003	T	C	10	GENIC	heterozygous	148549072
10	94649372	94649373	G	A	20	GENIC	homozygous	144083874
10	94655262	94655263	G	A	10	GENIC	homozygous	148549073
10	94663402	94663403	T	C	30	GENIC	homozygous	138854828
10	94669835	94669836	C		17	GENIC	homozygous	141037490
10	94670395	94670396	C	G	8	GENIC	heterozygous	403295728
10	94670394	94670395	C		8	GENIC	homozygous	403295725
10	94670394	94670395	C	G	8	GENIC	heterozygous	403295726
10	94670395	94670396	C		8	GENIC	homozygous	403295727
10	94682103	94682104	C		10	GENIC	heterozygous	403295731
10	94682103	94682104	C	G	10	GENIC	heterozygous	403295732
10	94687128	94687129	C	T	16	GENIC	homozygous	144083875
10	94688038	94688039	T		18	GENIC	heterozygous	138700339
10	94689876	94689877	A	T	14	GENIC	homozygous	154665441
10	94689876	94689877	A		14	GENIC	heterozygous	403295733
10	94690262	94690263	A	C	27	GENIC	homozygous	138854918
10	94693087	94693088	T	C	21	GENIC	homozygous	138854921
10	94693567	94693568	A	G	29	GENIC	homozygous	138854922
10	94693748	94693749	T	C	15	GENIC	homozygous	144083876
10	94694045	94694046	T	C	18	GENIC	homozygous	138854923
10	94695078	94695079	G	A	20	GENIC	homozygous	138854924
10	94695092	94695093	C	T	21	GENIC	homozygous	138854925
10	94695264	94695265	A	G	21	GENIC	homozygous	138854927
10	94695582	94695583	T	C	17	GENIC	homozygous	144083877
10	94696277	94696278	A	G	18	GENIC	homozygous	144083878
10	94696400	94696401	C		21	GENIC	homozygous	144078512
10	94696433	94696434	G	T	20	GENIC	homozygous	138854928
10	94697442	94697443	C	A	20	GENIC	homozygous	144083879
10	94697507	94697508	A	G	20	GENIC	homozygous	138854929