chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	45849763	45849763		GA	49	GENIC	homozygous	139171305
13	45850761	45850761		ACAT	36	GENIC	homozygous	139171306
13	45851543	45851544	T	C	47	GENIC	homozygous	139287175
13	45851768	45851769	A	G	61	GENIC	homozygous	139287176
13	45851892	45851893	C	T	71	GENIC	homozygous	139287177
13	45852521	45852522	T	A	47	GENIC	homozygous	139287179
13	45853888	45853889	A		40	GENIC	homozygous	139171307
13	45854440	45854441	G	A	59	GENIC	homozygous	139287185
13	45853331	45853332	C	T	18	GENIC	homozygous	139287182
13	45853393	45853394	G	C	31	GENIC	homozygous	139287183
13	45853813	45853814	A	G	40	GENIC	homozygous	139287184
13	45853289	45853290	T	C	28	GENIC	homozygous	142367977
13	45854512	45854513	C	T	52	GENIC	homozygous	142367978
13	45855076	45855077	C	T	49	GENIC	homozygous	142367979
13	45855291	45855292	T		5	GENIC	heterozygous	403648837
13	45855291	45855292	T	A	5	GENIC	heterozygous	403648838