chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106338269	106338270	A	T	17	GENIC	homozygous	51590538
10	106339683	106339685	GT	--	13	GENIC	heterozygous	52463031
10	106347076	106347077	C	-	6	GENIC	heterozygous	52813710
10	106347091	106347093	GT	--	3	GENIC	heterozygous	52447725
10	106354189	106354190	T	C	20	GENIC	homozygous	51590543
10	106362564	106362565	G	GTTT	26	GENIC	homozygous	51590545
10	106362572	106362573	G	GT	16	GENIC	heterozygous	52447729
10	106368841	106368842	T	TG	1	GENIC	homozygous	51590551
10	106374268	106374269	C	-	2	GENIC	homozygous	51590559
10	106384747	106384748	A	ATG	5	GENIC	homozygous	52407076
10	106384750	106384751	T	TGCTAGGCAAGCGCTCTACCACTGAGCTAAA	4	GENIC	homozygous	52407078
10	106384755	106384757	GG	--	5	GENIC	homozygous	52447731
10	106384758	106384759	G	-	5	GENIC	homozygous	51590577
10	106393629	106393630	T	-	11	GENIC	possibly homozygous	52447733
10	106394782	106394783	A	AT	10	GENIC	heterozygous	52734170
10	106402252	106402253	G	GA	20	GENIC	homozygous	51590581