chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	81924888	81924889	A	G	66	GENIC	homozygous	138834177
10	81925430	81925430		C	28	GENIC	homozygous	138694627
10	81925931	81925932	T	C	58	GENIC	homozygous	138834179
10	81926088	81926089	C	G	49	GENIC	homozygous	138834181
10	81926642	81926643	A	G	45	GENIC	homozygous	138834182
10	81926799	81926800	A	G	43	GENIC	possibly homozygous	138834183
10	81927410	81927411	A	G	41	GENIC	homozygous	138834184
10	81927982	81927983	C	T	33	GENIC	homozygous	138834186
10	81928475	81928476	C		11	GENIC	heterozygous	404016172
10	81928475	81928476	C	A	11	GENIC	possibly homozygous	404016173
10	81927500	81927501	T		40	GENIC	possibly homozygous	404016170
10	81927500	81927501	T	G	40	GENIC	heterozygous	404016171
10	81929599	81929600	G	T	60	GENIC	homozygous	138834187
10	81930186	81930187	T	C	49	GENIC	homozygous	138834188
10	81930420	81930421	T	C	52	GENIC	homozygous	138834189
10	81930479	81930480	A	G	46	GENIC	homozygous	138834190
10	81930380	81930381	G	A	52	GENIC	homozygous	143460024