chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94238734	94238735	T	C	25	GENIC	homozygous	117390115
9	94238781	94238782	T	C	23	GENIC	homozygous	117390117
9	94238917	94238918	G	A	19	GENIC	homozygous	117390118
9	94238963	94238964	A	G	21	GENIC	homozygous	117390120
9	94239001	94239002	C	T	27	GENIC	homozygous	117390121
9	94239134	94239135	G	A	13	GENIC	homozygous	117601963
9	94239188	94239189	T	C	26	GENIC	homozygous	117390123
9	94239326	94239327	G	A	18	GENIC	homozygous	117390124
9	94240989	94240990	C	T	20	GENIC	homozygous	117390126
9	94242072	94242073	G	C	16	GENIC	homozygous	117390128
9	94242332	94242333	A	G	17	GENIC	homozygous	117390129
9	94242364	94242365	A	C	25	GENIC	homozygous	117390131
9	94244297	94244298	G	C	23	GENIC	homozygous	117390133
9	94247507	94247508	G	A	19	GENIC	homozygous	117601965
9	94247630	94247631	A	C	21	GENIC	homozygous	117390134
9	94247969	94247970	A	G	38	GENIC	homozygous	117390136
9	94248057	94248058	A	T	28	GENIC	homozygous	117601967
9	94248484	94248485	C	G	13	GENIC	homozygous	117601969
9	94249423	94249424	T	C	27	GENIC	homozygous	117390138
9	94250831	94250832	C	T	21	GENIC	homozygous	117390139
9	94252124	94252125	A	G	26	GENIC	homozygous	117390141