chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	51960816	51960817	A	C	8	GENIC	homozygous	59693180
2	51960817	51960818	A	T	8	GENIC	homozygous	59693182
2	51961330	51961331	G	C	20	GENIC	possibly homozygous	59693184
2	51962055	51962056	A	G	5	GENIC	heterozygous	59693194
2	51962347	51962348	A	AC	18	GENIC	possibly homozygous	59693196
2	51962641	51962642	A	T	16	GENIC	homozygous	59693198
2	51962730	51962731	A	ATT	7	GENIC	possibly homozygous	59693200
2	51963003	51963004	G	A	19	GENIC	homozygous	59693202
2	51963081	51963082	G	A	17	GENIC	homozygous	59693204
2	51963298	51963299	G	A	23	GENIC	homozygous	59693206
2	51963489	51963490	T	C	11	GENIC	heterozygous	60113039
2	51964571	51964572	A	C	13	GENIC	homozygous	59693208
2	51966241	51966242	T	TA	5	GENIC	homozygous	59693212
2	51966986	51966990	TTGT	----	4	GENIC	heterozygous	59693214
2	51967658	51967659	C	A	26	GENIC	possibly homozygous	59693216
2	51967765	51967766	T	C	20	GENIC	homozygous	59693218
2	51968809	51968811	TT	--	1	GENIC	homozygous	59693220
2	51968955	51968956	C	T	13	GENIC	homozygous	59693222
2	51970355	51970356	A	G	16	GENIC	homozygous	59693228