chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	45849763	45849763		GA	57	GENIC	homozygous	139171305
13	45850761	45850761		ACAT	42	GENIC	homozygous	139171306
13	45851543	45851544	T	C	55	GENIC	homozygous	139287175
13	45851768	45851769	A	G	46	GENIC	homozygous	139287176
13	45851892	45851893	C	T	52	GENIC	homozygous	139287177
13	45852423	45852424	C	G	49	GENIC	homozygous	139287178
13	45852521	45852522	T	A	41	GENIC	homozygous	139287179
13	45853030	45853031	C	A	51	GENIC	homozygous	139287180
13	45853223	45853224	A	C	37	GENIC	possibly homozygous	139287181
13	45853331	45853332	C	T	13	GENIC	homozygous	139287182
13	45853393	45853394	G	C	24	GENIC	homozygous	139287183
13	45853813	45853814	A	G	32	GENIC	homozygous	139287184
13	45853888	45853889	A		46	GENIC	homozygous	139171307
13	45854440	45854441	G	A	54	GENIC	homozygous	139287185
13	45854893	45854894	C	A	48	GENIC	homozygous	139287186
13	45855291	45855292	T		10	GENIC	heterozygous	403648837
13	45855291	45855292	T	A	10	GENIC	heterozygous	403648838