chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	51649757	51649758	A	G	53	GENIC	homozygous	136106166
2	51652259	51652260	T	C	61	GENIC	homozygous	136106167
2	51652784	51652785	A	G	44	GENIC	homozygous	136106168
2	51653402	51653403	G	A	43	GENIC	homozygous	136106169
2	51654504	51654505	C	T	58	GENIC	possibly homozygous	136106170
2	51654893	51654893		A	59	GENIC	homozygous	135906831
2	51655177	51655178	C	T	70	GENIC	homozygous	136106171
2	51661183	51661184	T	C	48	GENIC	possibly homozygous	136106172
2	51661365	51661366	C	T	41	GENIC	homozygous	136106173
2	51661545	51661546	T	C	40	GENIC	homozygous	136106174
2	51663078	51663079	A	G	49	GENIC	homozygous	136106175
2	51666585	51666586	A	G	46	GENIC	homozygous	136106176
2	51654894	51654894		TTGACCAGATTCA	59	GENIC	homozygous	135906832
2	51657755	51657759	TGCC		48	GENIC	homozygous	135906833
2	51661794	51661794		A	57	GENIC	possibly homozygous	135906834