chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61414893	61414894	G	T	20	GENIC	homozygous	116612769
10	61415081	61415082	C	T	19	GENIC	homozygous	116939351
10	61415380	61415381	T	G	26	GENIC	possibly homozygous	116612771
10	61415705	61415706	T	C	25	GENIC	possibly homozygous	116939353
10	61416038	61416039	T	C	21	GENIC	homozygous	116939355
10	61416148	61416149	C	T	25	GENIC	homozygous	116939357
10	61416152	61416153	A	G	23	GENIC	homozygous	116939359
10	61416202	61416203	T	G	21	GENIC	homozygous	116790521
10	61417279	61417280	G	T	28	GENIC	homozygous	116939361
10	61418381	61418382	A	C	19	GENIC	homozygous	116612775
10	61418513	61418514	T	C	29	GENIC	homozygous	116939363
10	61418829	61418830	G	C	28	GENIC	homozygous	116939365
10	61419076	61419077	C	T	14	GENIC	homozygous	116939367
10	61419082	61419083	C	G	13	GENIC	homozygous	116939369
10	61419465	61419466	T	G	32	GENIC	homozygous	116612779
10	61419537	61419538	C	A	25	GENIC	homozygous	116790525
10	61419548	61419549	G	C	25	GENIC	homozygous	116790527
10	61419549	61419550	G	A	25	GENIC	homozygous	116939371
10	61419636	61419637	G	A	30	GENIC	homozygous	117079862
10	61419879	61419880	C	G	31	GENIC	homozygous	116612783
10	61419920	61419921	C	A	39	GENIC	homozygous	116612785
10	61420449	61420450	G	A	18	GENIC	homozygous	116612787
10	61421905	61421906	C	T	10	GENIC	homozygous	116939375