chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82056639	82056640	C	T	38	GENIC	heterozygous	51516476
10	82059064	82059065	C	T	29	GENIC	heterozygous	51516479
10	82060892	82060893	T	A	19	GENIC	heterozygous	51516488
10	82063582	82063583	G	T	38	GENIC	heterozygous	51516497
10	82063591	82063592	A	T	39	GENIC	heterozygous	51516498
10	82064237	82064238	C	T	10	GENIC	heterozygous	51516500
10	82072600	82072601	C	G	9	GENIC	heterozygous	51516534
10	82072632	82072633	G	A	8	GENIC	heterozygous	51516535
10	82072648	82072649	C	A	8	GENIC	heterozygous	51516536
10	82072697	82072698	A	G	5	GENIC	heterozygous	51516537
10	82099307	82099308	C	T	10	GENIC	heterozygous	51516593
10	82099728	82099729	A	G	10	GENIC	heterozygous	51516598
10	82099804	82099805	G	A	13	GENIC	heterozygous	51516599
10	82104387	82104388	T	TG	9	GENIC	heterozygous	51516605
10	82104404	82104405	G	C	15	GENIC	heterozygous	51516606
10	82105827	82105828	T	C	12	GENIC	heterozygous	51516609