chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	61510947	61510948	C	G	12	GENIC	homozygous	133251127
11	61512230	61512231	C	T	21	GENIC	homozygous	126333230
11	61517225	61517226	G	A	6	GENIC	heterozygous	133251128
11	61523273	61523274	T	C	13	GENIC	homozygous	126333238
11	61522787	61522788	A	G	2	GENIC	homozygous	116104954
11	61511598	61511599	G	A	66	GENIC	heterozygous	118183888
11	61511696	61511697	A	G	39	GENIC	heterozygous	118161863
11	61520736	61520737	T	C	39	GENIC	homozygous	116158172
11	61521232	61521233	A	C	66	GENIC	homozygous	116158174
11	61521385	61521386	G	A	63	GENIC	homozygous	116158176
11	61524302	61524303	T	A	44	GENIC	homozygous	116158180
11	61524728	61524729	G	A	58	GENIC	homozygous	116158182
11	61525634	61525635	T	A	51	GENIC	possibly homozygous	116158184
11	61528701	61528702	G	T	68	GENIC	homozygous	116158186
11	61529789	61529790	G	A	63	GENIC	homozygous	116158188
11	61521019	61521019		GT	6	GENIC	homozygous	133245461
11	61523273	61523273		C	13	GENIC	heterozygous	133245462
11	61526106	61526107	A		54	GENIC	homozygous	133245463
11	61528720	61528721	A		66	GENIC	homozygous	133245464
11	61529312	61529312		A	55	GENIC	homozygous	133245465