chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	60586528	60586529	C		12	GENIC	homozygous	138686296
10	60586892	60586893	T	G	6	GENIC	homozygous	142252138
10	60588198	60588198		G	13	GENIC	homozygous	138686297
10	60588710	60588715	AAAGA		24	GENIC	homozygous	138686298
10	60593613	60593619	CCACCA		15	GENIC	homozygous	138686300
10	60589123	60589124	T	C	23	GENIC	homozygous	138801415
10	60593098	60593099	C	T	23	GENIC	homozygous	138801416
10	60589374	60589375	T	G	4	GENIC	heterozygous	149236494
10	60589378	60589379	T	G	3	GENIC	heterozygous	149236495
10	60594690	60594691	A	T	14	GENIC	homozygous	138801417
10	60596256	60596257	G	A	26	GENIC	homozygous	138801418
10	60596669	60596670	C	T	14	GENIC	homozygous	138801419
10	60598992	60598993	T	C	9	GENIC	homozygous	138801420
10	60601177	60601178	C	T	29	GENIC	homozygous	142252139
10	60601801	60601806	CCCCA		9	GENIC	homozygous	138686302
10	60607364	60607365	C	T	28	GENIC	homozygous	138801422
10	60608021	60608022	T	C	11	GENIC	homozygous	138801423
10	60610981	60610981		ATTTTAAAGCTGCCACCAGA	26	GENIC	homozygous	138686304
10	60599174	60599175	A		12	GENIC	heterozygous	141037247
10	60612856	60612857	A	G	15	GENIC	homozygous	138801424
10	60614611	60614612	G	A	12	GENIC	heterozygous	154645733
10	60599338	60599339	G	T	15	GENIC	heterozygous	403901137
10	60599338	60599339	G		15	GENIC	heterozygous	403901138
10	60599339	60599340	G	T	15	GENIC	heterozygous	403901139
10	60599339	60599340	G		15	GENIC	heterozygous	403901140
10	60608021	60608022	T	G	11	GENIC	heterozygous	403288078
10	60614611	60614612	G		12	GENIC	homozygous	403288079
10	60599336	60599337	C	T	15	GENIC	heterozygous	140904548