chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	74041234	74041235	C	T	14	GENIC	homozygous	116277957
11	74041629	74041630	G	A	26	GENIC	homozygous	115990559
11	74041656	74041657	T	G	24	GENIC	homozygous	115990561
11	74042438	74042439	C	T	28	GENIC	homozygous	116277959
11	74042530	74042531	C	T	18	GENIC	homozygous	116277961
11	74042839	74042840	T	C	26	GENIC	homozygous	116054476
11	74043127	74043128	A	T	21	GENIC	homozygous	115990571
11	74043479	74043480	C	T	14	GENIC	homozygous	115990575
11	74043621	74043622	T	C	17	GENIC	homozygous	115990577
11	74044041	74044042	T	C	34	GENIC	homozygous	115990581
11	74044088	74044089	A	G	38	GENIC	homozygous	115990583
11	74045003	74045004	G	A	30	GENIC	homozygous	116277963
11	74045189	74045190	G	A	40	GENIC	homozygous	116277965
11	74045289	74045290	A	G	29	GENIC	homozygous	115990589
11	74046376	74046377	G	C	47	GENIC	homozygous	115990593
11	74046576	74046577	A	G	33	GENIC	homozygous	115990595
11	74046767	74046768	C	T	34	GENIC	homozygous	115990597
11	74046813	74046814	G	A	27	GENIC	homozygous	116277967
11	74046989	74046990	C	T	25	GENIC	homozygous	116277969
11	74047096	74047097	C	T	22	GENIC	homozygous	116054484
11	74048628	74048629	C	T	39	GENIC	homozygous	116277971
11	74048806	74048807	C	T	33	GENIC	homozygous	116277973
11	74048981	74048982	T	C	25	GENIC	homozygous	115990599
11	74049108	74049109	C	T	27	GENIC	homozygous	115990601
11	74049293	74049294	G	A	39	GENIC	homozygous	115990603
11	74050292	74050293	A	C	24	GENIC	homozygous	115990607
11	74051332	74051333	C	T	23	GENIC	homozygous	116277976
11	74051534	74051535	C	G	23	GENIC	homozygous	115990611
11	74051636	74051637	G	C	31	GENIC	homozygous	115990613
11	74051695	74051696	C	T	22	GENIC	homozygous	116277978