chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61414893	61414894	G	T	18	GENIC	homozygous	116612769
10	61414957	61414958	A	G	13	GENIC	homozygous	116939349
10	61415081	61415082	C	T	20	GENIC	homozygous	116939351
10	61415380	61415381	T	G	16	GENIC	homozygous	116612771
10	61415705	61415706	T	C	27	GENIC	homozygous	116939353
10	61416038	61416039	T	C	27	GENIC	homozygous	116939355
10	61416148	61416149	C	T	22	GENIC	homozygous	116939357
10	61416152	61416153	A	G	22	GENIC	homozygous	116939359
10	61416202	61416203	T	G	16	GENIC	homozygous	116790521
10	61417279	61417280	G	T	27	GENIC	homozygous	116939361
10	61418513	61418514	T	C	14	GENIC	homozygous	116939363
10	61418829	61418830	G	C	19	GENIC	homozygous	116939365
10	61419076	61419077	C	T	18	GENIC	homozygous	116939367
10	61419082	61419083	C	G	18	GENIC	homozygous	116939369
10	61419465	61419466	T	G	22	GENIC	homozygous	116612779
10	61419537	61419538	C	A	23	GENIC	homozygous	116790525
10	61419548	61419549	G	C	20	GENIC	homozygous	116790527
10	61419549	61419550	G	A	18	GENIC	homozygous	116939371
10	61419839	61419840	A	G	12	GENIC	homozygous	116939373
10	61419879	61419880	C	G	9	GENIC	homozygous	116612783
10	61420449	61420450	G	A	8	GENIC	homozygous	116612787
10	61421905	61421906	C	T	7	GENIC	homozygous	116939375